Table 1.
Chromosomal abnormalities associated with anophthalmia/microphthalmia [55,7].
Chromosomal Abnormality | Other Features |
Duplication 3q syndrome (3q21-ter dup) | Learning difficulties, growth deficiency, hypertrichosis, craniosynostosis, cardiac defects, chest deformities, genital abnormalities, umbilical hernia |
4p- (Wolf-Hirschhorn syndrome) | Growth deficiency, microcephaly, ocular hypertelorism, cranial asymmetry, learning difficulties, epilepsy, cleft lip/palate, anterior segment dysgenesis |
Duplication 4p syndrome | Learning difficulties, epilepsy, growth deficiency, obesity, microcephaly, characteristic faces, genital abnormalities, kyphoscoliosis |
Deletion 7p15.1-p21.1 | Cryptophthalmos, cleft lip/palate, choanal atresia |
Trisomy 9 mosaic syndrome | Joint contractures, congenital heart defects, prenatal growth deficiency, learning difficulties, micrognathia, kyphoscoliosis |
Duplication 10q syndrome | Ptosis, short palpebral fissures, camptodactyly, learning difficulties, prenatal growth deficiency, microcephaly, heart and kidney malformations |
13q-, 13 ring | Microcephaly, learning difficulties, bilateral retinoblastoma, cardiac defects, hypospadias, cryptorchidism |
Trisomy 13 (Patau syndrome) | Holoprosencephaly, moderate microcephaly, coloboma, retinal dysplasia, cyclopia, cleft lip/palate, cardiac defects, genital abnormalities, 86% die within one year. |
Deletion 14q22.1-q23.2 | Pituitary hypoplasia. |
18q- | Midface hypoplasia, small stature, learning difficulties, hypotonia, nystagmus, conductive deafness, microcephaly, midface hypoplasia, genital abnormalities |
Trisomy 18 (Edwards syndrome) | Polyhydramnios, single umbilical artery, small placenta, low foetal activity, learning difficulties, hypertonicity, hypoplasia of skeletal muscle, subcutaneous, adipose tissue, prominent occiput, low-set malformed auricles, micrognathia, cardiac defects |
Triploidy syndrome | Large placenta with hydatidiform changes, growth deficiency, syndactyly, congenital heart defects, brain anomalies/holoprosencephaly |