Anophthalmia including next-generation sequencing-based approaches

Abstract

Name of the disease (synonyms)

See Table 1, Column 1—“Name of disease” and Column 2—“Alternative names”.

OMIM# of the disease

See Table 1, Column 3—“OMIM# of the disease”.

Name of the analysed genes or DNA/chromosome segments and OMIM# of the gene(s)

Core genes (irrespective of being tested by Sanger sequencing or next-generation sequencing):

See Table 1, Column 4—“Cytogenetic location”, Column 5—“Associated gene(s)” and Column 6—“OMIM# of associated gene(s)”.

Additional genes (if tested by next-generation sequencing, including Whole exome/genome sequencing and panel sequencing):

See Table 2, Column 1—“Gene”, Column 2—“Alternative names”, Column 3—“OMIM# of gene” and Column 4—“Cytogenetic location”.

Review of the analytical and clinical validity as well as of the clinical utility of DNA-based testing for mutations in the gene(s) in diagnostic, predictive and prenatal settings, and for risk assessment in relatives.

1. Disease characteristics

1.1 Name of the disease (synonyms)

See Table 1, Column 1—“Name of disease” and Column 2—“Alternative names”.

Table 1.

Overview of disease associated with non-syndromic and syndromic anophthalmia/severe microphthalmia

Name of disease	Alternative names	OMIM# of the disease	Cytogenetic location	Associated gene(s)	OMIM# of associated gene(s)	Inheritance
Aniridia 1 (AN1)	Cataract, congenital, with late-onset corneal dystrophy	106210	11p13	PAX6	607108	Autosomal dominant
Bosma arhinia microphthalmia syndrome (BAMS)	Arhinia, choanal atresia, microphthalmia and hypogonadotropic hypogonadism	603457	18p11.32	SMCHD1	614982	Autosomal dominant
Branchiooculofacial syndrome	BOF syndrome Branchial clefts with characteristic facies, growth retardation, imperforate, nasolacrimal duct and premature aging Hemangiomatous brancial clefts lip pseudocleft syndrome Lip pseudocleft hemangiomatous branchial cyst syndrome	113620	6p24.3	TFAP2A	107580	Autosomal dominant
Cerebrooculonasal syndrome	–	605627	Unknown	–	Unknown	Unknown
Chromosome 1q41-q42 deletion syndrome	Holoprosencephaly 10 (HPE10)	612530	1q41-q42	–	–	Isolated cases
COMMAD syndrome	Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness	617306	3p13	MITF	156845	Autosomal recessive
Dextrocardia with unusual facies and microphthalmia	–	221950	Unknown	–	–	Unknown
Focal dermal hypoplasia (FDH)	FODH DHOF Goltz syndrome Goltz-gorlin syndrome	305600	Xp11.23	PORCN	300651	X-linked dominant
Fraser syndrome 1 (FRASRS1)	Fraser syndrome Cryptophtalmos with other malformations Cryptophthalmos- syndactyly syndrome	219000	4q21.21	FRAS1	607830	Autosomal recessive
Fryns microphthalmia syndrome	Microphthalmia with facial clefting Anophthalmia-plus syndrome	600776	Unknown	–	–	Autosomal recessive
Fryns syndrome (FRNS)	Diaphragmatic hernia, abnormal face, and distil limb anomalies	229850	Unknown	–	–	Unknown
Holoprosencephaly 9 (HPE9)	Pituitary anomalies with holoprosencephaly-like features Holosproencephaly with microphthalmia and first branchial arch anomalies	610829	2q14.2	GLI2	165230	Autosomal dominant
Joubert syndrome 21	–	615636	8q13.1-q13.2	CSPP1	611654	Autosomal recessive
Kapur-toriello syndrome	Long columella with cleft lip/palate and eye, heart and intestinal anomalies	244300	Unknown	–	–	Unknown
Linear skin defects with multiple congenital anomalies 1 (LSDMCA1)	Microphthalmia, syndromic 7 (MCOPS7) Microphthalmia with linear skin defects (MLS) Microphthalmia, dermal aplasia, and sclerocornea Midas syndrome	309801	Xp22.2	HCCS	300056	X-linked dominant
Manitoba oculotrichoanal syndrome (MOTA)	Marles syndrome	248450	9q22.3	FREM1	608944	Autosomal recessive
Meckel syndrome, type 8 (MKS8)	–	613885	12q24.31	TCTN2	613846	Autosomal recessive
Microphthalmia with limb anomalies (MLA)	Waardenburg anophthalmia syndrome Anophthalmia- syndactyly Ophthalmoacromelic syndrome (OAS)	206920	14q24.2	SMOC1 FNBP4	608488 615265	Autosomal recessive
Microphthalmia, isolated 1 (MCOP1)	MCOP Anophthalmia, clinical, isolated Microphthalmos, autosomal recessive	251600	14q32	–	–	Autosomal recessive
Microphthalmia, isolated 2 (MCOP2)	Anophthalmia, clinical, isolated	610093	14q24.3	VSX2	142993	Autosomal recessive
Microphthalmia, isolated 3 (MCOP3)	–	611038	18q21.32	RAX	601881	Autosomal recessive
Microphthalmia, isolated 4 (MCOP4)	–	613094	8q22.1	GDF6	601147	Autosomal dominant
Microphthalmia, isolated 8 (MCOP8)	–	615113	15q26.3	ALDH1A3	600463	Autosomal recessive
Microphthalmia, isolated, with coloboma 3 (MCOPCB3)	Microphthalmia, cataracts and iris abnormalities	610092	14q24.3	VSX2	142993	Autosomal recessive
Microphthalmia, isolated with coloboma 4 (MCOPCB4)	–	251505	Unknown	–	–	Unknown
Microphthalmia, isolated, with coloboma 10 (MCOPCB10)	–	616428	10q23.33	RBP4	180250	Autosomal dominant
Microphthalmia, syndromic 1 (MCOPS1)	Lenz microphthalmia syndrome Lenz dysplasia MAA	309800	Xq28	NAA10	300013	X-linked dominant and recessive
Microphthalmia, syndromic 2 (MCOPS2)	Oculofaciocardiodental syndrome OFCD syndrome Microphthalmia, cataracts, radiculomegaly and septal heart defects ANOP2 MAA2 Lenz microphthalmia syndrome	300166	Xp11	BCOR	300485	X-linked dominant and recessive
Microphthalmia, syndromic 3 (MCOPS3)	Microphthalmia and esophageal atresia syndrome Clinical anophthalmia with assosicated anomalies Anophthalmia-esophageal genital syndrome AEG syndrome	206900	3q26.33	SOX2	184429	Autosomal dominant
Microphthalmia, syndromic 4 (MCOPS4)	Microphthalmia with ankyloblepharon and mental retardation Microphthalmia-ankyloblepharon-intellectual disability syndrome ANOP1	301590	Xq27-q28	–	–	X-linked recessive
Microphthalmia, syndromic 5 (MCOPS5)	Retinal dystrophy, early-onset, with or without pituitary dysfunction	610125	14q22.3	OTX2	600037	Autosomal dominant
Microphthalmia, syndromic 6 (MCOPS6)	Microphthlamia and pituitary anomalies Microphthalmia with brain and digit developmental anomalies Anophthalmia, clinical, with micrognathia, malformed ears, digital anomalies, and abnormal external genitalia	607932	14q22.2	BMP4	112262	Autosomal dominant
			14q23.1	SIX6	606326	Autosomal recessive
Microphthalmia, syndromic 9 (MCOPS9)	Anophthalmia, clinical, with mild facial dysmorphism and variable malformations of the lung, heart and diaphragm Anophthalmia/microphthalmia and pulmonary hypoplasia Pulmonary hypoplasia- diaphragmatic hernia- anophthalmia-cardiac defect (PDAC) Spear syndrome Matthew-wood syndrome Pulmonary agenesis, microphthalmia and diaphragmatic defect (PMD) Microphthalmia isolated with coloboma 8 (MCOPCB8)	601186	15q24.1	STRA6	610745	Autosomal recessive
Microphthalmia, syndromic 11 (MCOPS11)	–	614402	10q25.3	VAX1	604294	Autosomal recessive
Microphthalmia, syndromic 12 (MCOPS12)	Microphthalmia with or without pulmonary hypoplasia diaphragmatic hernia and/or cardiac defects Matthew-wood syndrome	615524	3p24.2	RARB	180220	Autosomal dominant and recessive
Microphthalmia/coloboma and skeletal dysplasia syndrome (MCSKS)	Microphthalmia or coloboma with or without rhizomelic skeletal dysplasia Microphthalmia, syndromic 14 (MCOPS14)	615877	4q31.3	MAB21L2	604357	Autosomal dominant and recessive
Oculocerebrocutaneous syndrome (OCCS)	Orbital cyst with cerebral and focal dermal malformations Delleman syndrome	164180	Unknown	–	–	Unknown
Sakoda complex	Sphenoethmoidal encephalomeningocele agenesis of the corpus callosum and cleft lip/palate Sakoda spectrum	610871	Unknown	–	–	Unknown
Short-rib thoracic dysplasia 12 (SRTD12)	Short rib-polydactyly syndrome, type IV (SRPS4) Beemer-langer syndrome Short rib syndrome, beemer type	269860	Unknown	–	–	Unknown
Thoracoabdominal syndrome (THAS)	Midline defects, X-linked Pentalogy of cantrell	313850	Xq25-q26.1	–	–	X-linked

1.2 Online Mendelian Inheritance in Man (OMIM)# of the disease

See Table 1, Column 3—“OMIM# of the disease”.

1.3 Name of the analysed genes or DNA/chromosome segments and OMIM# of the gene(s)

1.3.1 Core genes (irrespective of being tested by Sanger sequencing or next-generation sequencing)

See Table 1, Column 4—“Cytogenetic location”, Column 5—“Associated gene(s)” and Column 6—“OMIM# of associated gene(s)”.

1.3.2 Additional genes (if tested by next-generation sequencing, including whole exome/genome sequencing and panel sequencing)

See Table 2, Column 1—“Gene”, Column 2—“Alternative names”, Column 3—“OMIM# of gene” and Column 4—“Cytogenetic location”.

Table 2.

Additional genes associated with anophthalmia/severe microphthalmia, tested by next-generation sequencing

Gene	Alternative names	OMIM# of gene	Cytogenetic location
BMP7	–	112267	20q13.31
YAP1	–	606608	11q22.1
TBC1D32	C6orf170 BROMI	615867	6q22.31

1.4 Mutational spectrum

“True anophthalmia” is defined as abortion of eye development at the stage of the developing optic vesicle (3–4 weeks gestation) leading to absence of the eye, optic nerve and chiasm. However, more commonly “clinical anophthalmia” (often interchangeable with the term “severe microphthalmia”, see Clinical Utility Gene Card for non-syndromic microphthalmia [1]) occurs, where a small cystic remnant is detectable on pathology/imaging. Clinical anophthalmia is caused by the degeneration of the optic vesicle after it has formed, leading to the presence of a hypoplastic optic nerve, chiasm or tract. Anophthalmia is part of the phenotypic continuum with microphthalmia and coloboma, and can manifest bilaterally or unilaterally (with the contralateral eye exhibiting associated ocular anomalies [complex], such as ocular coloboma, microphthalmia, cataract and anterior segment dysgenesis) [2, 3]. In 33–95% of anophthalmia and microphthalmia, associated systemic anomalies can be found, however, only 20–45% are the result of a known syndrome [2–4]. The most common extraocular features associated with anophthalmia/microphthalmia are craniofacial (including the face, ear and neck), limb and musculoskeletal anomalies [4–7].

A complex aetiology exists with chromosomal, monogenic and environmental causes identified. Chromosomal anomalies, including aneuploidy, triploidy, translocations, deletions and duplications account for 20–30% of anophthalmia/microphthalmia patients [2, 3, 8, 9]. Anophthalmia is clinically and genetically heterogeneous, and may be inherited through recessive (biallelic) or dominant modes, although most cases of non-syndromic anophthalmia are sporadic and monoallelic resulting in haploinsufficiency, such as with PAX6 and SOX2. The occurrence of de novo changes, mosaicism and non-penetrance makes prediction of the inheritance pattern difficult. Diagnosis through molecular/genetic testing including next-generation sequencing and array comparative genomic hybridisation (aCGH), can identify the genetic basis of bilateral anophthalmia or severe microphthalmia in 80% of cases, but this is considerably lower for unilateral cases (<10%) [1, 2, 10]. The low diagnostic frequency of unilateral anophthalmia/severe microphthalmia indicates only a small number of disease-associated genes have been identified, which is not surprising given the complexity of eye development [9]. Advances in next-generation sequencing technology will allow for the identification of previously unknown deletions, duplications, inversions and translocations, as well as non-coding and splice variants [11]. Whole exome sequencing/whole genome sequencing (WES/WGS) screens all coding genes/the whole genome, which can increase the identification of novel disease-associated variants, including genes in associated loci where no candidate gene has yet been identified (Table 1), as well as eliminate loci which have been incorrectly associated with a disease [9, 12].

The major genes associated with anophthalmia broadly fall into two distinct categories (i) eye field initiating transcription factors, such as SOX2 (OMIM: 184429) and OTX2 (OMIM: 600037), or (ii) retinoic acid signalling pathway components, including STRA6 (OMIM: 610745), ALDH1A3 (OMIM: 600463) and RARB (OMIM: 180220) [10, 13, 14].

Approximately 75% of incidences of bilateral anophthalmia or severe microphthalmia carry monoallelic (heterozygous) loss-of-function variants in SOX2 or OTX2, or biallelic (homozygous or compound heterozygous) loss-of-function variants in STRA6 [10, 15]. A wide spectrum of variants have been implicated in anophthalmia, however, molecular analyses with larger patient cohorts from a range of different ethnic backgrounds is required to detect novel variants and more accurately estimate their relative contribution (Table 1, Table 2) [7, 10, 16–19].

The most common cause of bilateral anophthalmia and severe microphthalmia are heterozygous variants of SOX2, with 76 known variants (63 of which are loss-of-function deletion, frameshift and nonsense) accounting for up to 40% of cases [4, 10, 15]. The most common SOX2 variant is the deletion (NM_003106.3) c.70_89del20 (p.Asn24Argfs*) [10]. The majority of variants (60%) arise de novo, while 8% are known to be inherited [10]. Autosomal dominant inheritance of disease-associated SOX2 variants can be from an affected, non-penetrant or mosaic parent [4, 10, 20–22]. Haploinsufficiency of SOX2 can cause isolated unilateral or bilateral anophthalmia, in addition to Syndromic Microphthalmia 3, where extraocular features include brain anomalies, neurocognitive delays, seizures, sensorineural hearing loss, oesophageal atresia, short stature, microcephaly and genital anomalies [4, 23].

Heterozygous variants in OTX2 are the second most prevalent cause of anophthalmia, with 47 known variant alleles, 38 of which are loss-of-function variants including indel, frameshift and nonsense [4, 10]. Approximately 40% of OTX2 variants arise de novo and 35% are inherited [10, 15, 24]. The frequency of non-penetrance and variable expressivity is high with OTX2 changes [10, 15, 24–26]. There have also been multiple confirmed cases of gonadal mosaicism [10, 15, 24–26]. A recent study reported that for 69 microphthalmia, anophthalmia and coloboma (MAC) patients with an OTX2 variant, in ten cases a heterozygous OTX2 variant was transmitted from an unaffected parent, compared with eight cases of inheritance from an affected parent [10]. In 2011, it was found that 2/3rds of reported parents carrying OTX2 mutations were unaffected due to mosaicism or non-penetrance [24]. The frequency of variable expressivity, non-penetrance and mosaicism for OTX2 variants may have implications for genetic counselling [25]. Patients with OTX2 associated anophthalmia/severe microphthalmia display extremely variable phenotypes, with complex ocular abnormalities including anterior segment dysgenesis, retinal dystrophy and hypoplasia or aplasia of the optic nerve and optic chiasm, and syndromic features including pituitary abnormalities, hypopituitarism, brain anomalies, seizures and developmental delay [4, 24, 27, 28].

Biallelic RAX loss-of-function variants account for 2–3% of anophthalmia and microphthalmia, and include missense, nonsense, frameshift and splicing variants, as well as whole gene deletions [1, 10, 29–31]. Monoallelic carriers of RAX variants display no ocular phenotype, while patients with biallelic changes are usually associated with bilateral severe microphthalmia, alongside neurological features such as intellectual deficiency and autism [10, 30, 31].

Monoallelic loss-of-function PAX6 changes account for 1–2% of MAC, and are commonly associated complex ocular features, including aniridia, although infrequently associated with systemic abnormalities [10]. Biallelic cases of PAX6, such as compound heterozygous variants, usually result in termination of pregnancy or neonatal death [10].

Variants in STRA6 can contribute to bilateral anophthalmia, with 11 known missense and 15 loss-of-function [10]. STRA6 changes which alter function can cause both non-syndromic and syndromic anophthalmia, including Syndromic Microphthalmia 9 (OMIM: 601186), where termination of pregnancy or death is seen within the first 2 years of life [10, 32–34].

ALDH1A3 variants have been estimated to occur in up to 10% of patients with bilateral anophthalmia and microphthalmia, with 11 identified disease-associated variants described [10, 35–37]. There has been a report of non-penetrance, and although systemic abnormalities are rare, there is an association with behavioural problems such as autism [37, 38].

Monoallelic and biallelic RARB alleles can cause anophthalmia/microphthalmia due to a loss-of-function (such as (NM_000965.3) c.355C>T (p.Arg119*)) or gain-of-function (such as (NM_000965.3) c.1159C>T (p.Arg387Cys)) [13, 14, 35]. Disease-associated RARB variants have been associated with Syndromic Microphthalmia 12, resulting in the termination of pregnancy, neonatal death, or severe developmental delay in those patients who survive the neonatal period [13, 14].

Only 1% of MAC cases screened for GDF6 found a disease-associated change, but variants are associated with bilateral anophthalmia or severe microphthalmia [10, 16]. Variants of GDF6 are associated with Klippel Feil syndrome, where systemic features include congenital fusion of the cervical spine vertebrae, a low posterior hairline and a short neck with limited mobility [5].

All data were mined from primary literature or curated genomic and phenotype databases, including Online Mendelian Inheritance in Man, OMIM (http://omim.org/); ClinVar, public archive of interpretations of clinically relevant variants (http://www.ncbi.nlm.nih.gov/clinvar/); Gene Reviews (http://www.ncbi.nlm.nih.gov/books/NBK1116/) and OrphaNet (https://www.orpha.net/consor/cgi-bin/Disease.php?lng=EN). Novel data should be shared through these databases. They were last accessed on 09 January 2019.

1.5 Analytical validation

Sequencing of both DNA strands. Disease-associated variants should be confirmed using genomic DNA from a new extraction. Disease-associated variants found with next-generation sequencing should be verified using Sanger sequencing or other specific molecular methods (e.g., PCR digest); for further details, see the Eurogentest Guideline [39]. It is important to look for segregation to determine whether the variant is de novo in isolated cases, providing a higher likelihood that it affects function. In clinical practice, aCGH or multiplex ligation-dependent probe amplification assay may be performed initially to detect deletions or duplications. Some molecular service labs also offer fluorescence in situ hybridisation to identify rearrangements or copy-number variation.

1.6 Estimated frequency of the disease

(Incidence at birth (“birth prevalence”) or population prevalence. If known to be variable between ethnic groups, please report):

The reported birth prevalence of anophthalmia ranges from 0.18 to 0.6 per 10,000, which is consistent across most countries [10, 17, 40–42]. In a prospective UK childhood incidence study of MAC cases (11.9 per 100,000), clinical anophthalmia was rare, being present in only 5.2% (7/135) of children under 16 [18]. Of the anophthalmic cases, two were bilateral, three were unilateral and two had microphthalmia or coloboma in the contralateral eye [8]. This study found significant ethnicity differences in the annual live birth incidence, however, these associations may be confounded by socioeconomic status [18]. There is no evidence of gender predilection.

Multiple births, maternal age over 40, low birthweight and low gestational age are associated risk factors for anophthalmia [6, 7, 18, 40]. Furthermore, maternal smoking during early pregnancy, exposure to certain medications (including the antibiotic nitrofurantoin) during early pregnancy and maternal viral infections (including rubella, CMV and influenza) may increase the likelihood of having a child with anophthalmia [41, 43–47].

1.7 Diagnostic setting

	Yes.	No.
A. (Differential) diagnosis	⊠	☐
B. Predictive testing	⊠	☐
C. Risk assessment in relatives	⊠	☐
D. Prenatal	⊠	☐

Because of the time constraints of pregnancy, panel diagnostic or WES/WGS filtering is preferred if there is a request for prenatal diagnosis.

2. Test characteristics

	Genotype or disease		A: True positives	C: False negative
	Present	Absent	B: False positives	D: True negative
Test
Pos.	A	B	Sensitivity Specificity	A/(A + C) D/(D + B)
Neg.	C	D	Pos. predict value Neg. predict value	A/(A + B) D/(C + D)

2.1 Analytical sensitivity

(Proportion of positive tests if the genotype is present in the analyte.)

2.1.1 If tested by conventional Sanger sequencing

Less than 100%. The proportion is likely <100%, because primers may be localised on sequences containing SNVs or rare variants, which results in a preferential amplification of one allele (allele dropout). A supplementary deletion/duplication diagnostic test should be performed for genes with a known proportion of large genomic deletions/duplications as outlined in the section “Analytical validation”.

2.1.2 If tested by next-generation sequencing

Less than 100%. The proportion is likely <100%, because there might be disease-associated variants in regions that could not be enriched and/or sequenced by next-generation sequencing owing to suboptimal coverage of some regions of interest with this technology depending on next-generation sequencing strategy. If amplicon-based enrichment strategies are being used, primers may be localised on SNVs or rare variants, which results in preferential amplification of one allele. In patients with a highly suggestive phenotype in whom testing for specific gene alterations proves negative, a supplementary deletion/duplication diagnostic test should be performed for genes with a known proportion of large genomic deletions/duplications as outlined in the section “Analytical validation”.

2.2 Analytical specificity

(Proportion of negative tests if the genotype is not present.)

2.2.1 If tested by conventional Sanger sequencing

Nearly 100%. False positives may arise owing to misinterpretation of rare polymorphic variants.

2.2.2 If tested by next-generation sequencing

Less than 100%. The risk of false positives owing to misinterpretation of rare polymorphic variants may be higher compared with Sanger sequencing because of greater number of analysed genes.

2.3 Clinical sensitivity

(Proportion of positive tests if the disease is present.)

2.3.1 If tested by conventional Sanger sequencing

Of those patients that undergo genetic testing of known causative genes with Sanger sequencing, <10% of patients with unilateral isolated anophthalmia will receive a molecular diagnosis. Those with bilateral severe cases will have a 75% diagnostic rate if aCGH and the coding regions of the following four genes are screened; SOX2, OTX2, PAX6 and STRA6 [15].

2.3.2 If tested by next-generation sequencing

See section “If tested by conventional Sanger sequencing”. Variant detection rates are higher when WES is combined with aCGH and high-resolution analysis of intragenic microdeletions and microduplications are performed. WGS may aid in the detection of function-affecting variants in the promotor region, introns and other non-coding regulatory elements, and provide better coverage than exome sequencing. Regulatory element disruption in anophthalmia remains largely uncharacterised.

2.4 Clinical specificity

(Proportion of negative tests if the disease is not present.)

2.4.1 If tested by conventional Sanger sequencing

Unknown, however, if anophthalmia is not present, it is unlikely that a positive test will be detected.

2.4.2 If tested by next-generation sequencing

See section “If tested by conventional Sanger sequencing”.

2.5 Positive clinical predictive value

(Lifetime risk to develop the disease if the test is positive.)

Anophthalmia is a congenital anomaly; hence, patients will be born with this defect, therefore nearly 100%.

2.6 Negative clinical predictive value

(Probability not to develop the disease if the test is negative.)

Nearly 100% as a congenital anomaly (but need to check no evidence of microphthalmia through axial length measurements).

Index case in that family had been tested:

Nearly 100%. If the non-affected relative is not a carrier of an identified disease-associated variant, they have no increased risk, except a small risk related to the prevalence in the general population.

Index case in that family had not been tested:

Unknown.

3. Clinical utility

3.1 (Differential) diagnostics: the tested person is clinically affected

(To be answered if in 1.9 “A” was marked)

3.1.1 Can a diagnosis be made other than through a genetic test?

No.	☐ (Continue with 3.1.4)
Yes.	⊠
	Clinically	⊠
	Imaging	⊠
	Endoscopy	☐
	Biochemistry	☐
	Electrophysiology	☐
	Other (please describe)

3.1.2 Describe the burden of alternative diagnostic methods to the patient

Prenatal diagnosis can be performed through 2D or 3D ultrasonography during the second trimester (or at 12 weeks post-conception with a transvaginal ultrasound) or foetal magnetic resonance imaging (MRI) to visualise the orbit [2, 48–50]. However, ultrasound examination may appear normal in affected foetuses, particularly in early scans where eye development is arrested after initial formation of the early eye cup [51].

Postnatal diagnosis can be made through clinical examination. In order to define whether anophthalmia is “true” or “clinical/severe microphthalmia”, MRI brain and orbit imaging can be used to determine the absence of the globe, optic nerve and optic chiasm or amorphous tissue with a hypoplastic optic nerve, respectively [2, 52].

A diagnosis of anophthalmia can be made relatively easily and cost-effectively, but if this anomaly is seen, children should be investigated within a multidisciplinary team, including paediatricians and clinical geneticists, to ensure this is not part of a syndrome. Further monitoring may be required as syndromic manifestations may present later in childhood.

3.1.3 How is the cost effectiveness of alternative diagnostic methods to be judged?

Clinical examination and ultrasound imaging provides a cost-effective diagnosis [1].

3.1.4 Will disease management be influenced by the result of a genetic test?

No.	☐
Yes.	⊠
	Therapy (please describe)	–
	Prognosis (please describe)	Yes, if a variant in a gene is associated with a syndrome, it may lead to further investigations for systemic involvement to prevent morbidity and maximise function, e.g., patients with SOX2 anophthalmia syndrome suffer from a range of multisystem abnormalities including seizures and sensorineural deafness, hence early diagnosis will lead to prompt supportive treatment, having long term health economic benefits.
	Management (please describe)	Anophthalmia should be managed by specialists with expertise in this condition. Socket expansion using enlarging conformers can minimise facial deformity, which can be started very soon after birth. In patients with anophthalmia, there is often an underdevelopment of the bony orbit, eyelid or fornices. Without intervention, the socket remains underdeveloped and prevents the ability for prosthesis later in life. In addition, in unilateral cases may lead to more pronounced facial asymmetry. The cosmetic deformity may result in psychological stress for the patient in the social environment. Introduction of socket expanders to add volume to the socket facilitates the progressive growth. In addition, supportive treatment for associated systemic abnormalities identified by genetic diagnosis must be monitored e.g., reversal of sleep pattern treated with melatonin supplements, growth assessment due to pituitary abnormalities, such as in the case of SIX6 variants [52]. Genetic counselling should be provided for the patient and family where appropriate, especially if the mode of inheritance can be identified [2].

3.2 Predictive setting: the tested person is clinically unaffected but carries an increased risk based on family history

(To be answered if in 1.9 “B” was marked.)

3.2.1 Will the result of a genetic test influence lifestyle and prevention?

If the test result is positive (please describe):

Anophthalmia is a congenital eye anomaly, therefore, if it is not clinically present at birth then this will not develop later in life. However, if an individual is clinically unaffected but a carrier, this information will inform family planning if the mode of inheritance can be identified.

If the test result is negative (please describe):

If the clinically unaffected person has a negative test result, no further follow-up is required. The result will inform family planning.

3.2.2 Which options in view of lifestyle and prevention does a person at-risk have if no genetic test has been done (please describe)?

A patient with anophthalmia has no vision in the affected eye. If there is bilateral involvement, in addition to other syndromic features, this may impact all aspects of lifestyle including schooling and future profession. Hence, a clinical diagnosis can help to provide support from an early age for both the patient and family, at home and at school, and guide career and work choices.

3.3 Genetic risk assessment in family members of a diseased person

(To be answered if in 1.9 “C” was marked.)

3.3.1 Does the result of a genetic test resolve the genetic situation in that family?

Yes, although there may be variable expressivity, non-penetrance and germline mosaicism, which will complicate the advice that can be given.

3.3.2 Can a genetic test in the index patient save genetic or other tests in family members?

If a disease-associated change is identified in the index patient, family members can be tested, but ophthalmic examination is also helpful, for example to ascertain microphthalmia or other related ocular features on the phenotypic continuum. Test negative family members, who are clinically unaffected, do not need any further investigation or monitoring.

3.3.3 Does a positive genetic test result in the index patient enable a predictive test in a family member?

Yes, if the variant is known.

3.4 Prenatal diagnosis

(To be answered if in 1.9 “D” was marked.)

3.4.1 Does a positive genetic test result in the index patient enable a prenatal diagnosis?

Yes. Germline mosaicism and/or non-penetrance render the prediction of recurrence risk difficult in monogenic anophthalmic individuals; however, molecular genetic studies for known variants are possible on amniotic fluid foetal cells withdrawn after 14 weeks of gestation or on chronic villus sampling at 10–12 weeks gestation, and can facilitate the diagnosis of anophthalmia [1, 2, 51]. In addition, transvaginal ultrasonography enables the detection of anophthalmia from 12 weeks gestation, through 2D or 3D ultrasonography during the second trimester or using foetal MRI to visualise and analyse the orbit of a foetus [2, 48–50].

Non-invasive prenatal diagnosis of aneuploidies and some monogenic disorders can be achieved by molecular testing of cell-free foetal DNA (cffDNA) from maternal plasma [53–58]. While non-invasive prenatal diagnosis of anophthalmia is not currently available, the reduced risk of non-invasive, early screening (7–9 weeks), makes cffDNA a valuable emerging tool for diagnosis of genetic disorders, particularly for patients with known risk [53, 54].

4. If applicable, further consequences of testing

Please assume that the result of a genetic test has no immediate medical consequences. Is there any evidence that a genetic test is nevertheless useful for the patient or his/her relatives? (Please describe)

Identifying the genetic cause can aid in identifying additional syndromic features in addition to guiding genetic counselling by identifying the mode of inheritance. Preimplantation diagnosis may be an option for bilateral anophthalmia/severe microphthalmia.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.