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. 2021 Feb 5;12:833. doi: 10.1038/s41467-021-21053-2

Table 1.

Phenotypes of patients with EIF5A variants.

Characteristics Individual
1 2 3 4 5 6 7
Sex (age)a F (6.9 y) F (8.4 y) F (8.4 y) M (18.3 y) M (8 mo) M (4 y) F (16.4 y)
Genomic positionb 17:7213097 17:7214714 17:7214722 17:7214723 17:7214723 17:7214741 17:7214762
cDNAc protein consequenced c.143C>A p.T48N c.316G>A p.G106R c.324dupA p.R109Tfs*8 c.325C>G p.R109G c.325C>T p.R109* c.343C>T p.P115S c.364G>A p.E122K
Inheritance/zygosity DN Het DN Het DN Het DN Het DN Het DN Het DN Het
Perinatal history
  Congenital microcephaly Yes Yes Yes Unknown No No Unknown
  IUGR Yes Yes No Yes No No No
  Feeding difficulties No Yes Yes Yes Yes No No
  Other No Cardiac anomalies

Cardiac anomalies

Cleft palate

Hypotonia

Cardiac anomalies

Hypotonia

No Foetal ascites
DD/ID Moderate/severe Moderate Mild Moderate Moderate Mild/Moderate Moderate
CNS anomalies No No No Peritrigonal hyperintensities No Left lateral ventriculomegaly No
Physical anomalies
  Heart No Yes Yes Unknown Yes Unknown Unknown
  Craniofacial Yes No Yes Yes Yes No No
  Other Hemivertebrae (L3) No No

Cryptorchidism

Pes planus

No No

Toe contractures

Small toenails

Pes planus

Growth parameters
  Height (SD) N (0.53) SS (−2.82) N (0.86) N (−0.45) N (−1.45) N (+1 SD), SS (−2.59)
  Weight (SD) OW (2) LW (−2.28) N (−0.41) N (0.06) LW (−3.14) N (−0.09 SD) N (−0.69)
  HC (SD) Mi (−3) Mi (−7.47) Mi (−2.11) Mi (−2.62) N (−0.45) N (−1.09) Mi (−1.94)
Facial dysmorphisms
  Broad eyebrows Yes Yes Yes Yes No Yes No
 Abn. supraorbital ridges Yes Yes Yes Yes No No No
 Epi/telecanthus No Yes Yes Yes Yes No Yes
 Bulbous nasal tip Yes Yes Yes Yes No No No
 Thin upper lip No Yes Yes Yes Yes No No
 Micrognathia Yes Yes Yes Yes No Yes No
 Low set ears Yes Yes No No No No Yes
 Other Lower eyelid hypoplasia Hypertelorism No Prominent long ears Plagiocephaly Sparse scalp hair Frontal bossing Downslanting PF Cupped ears Long PF hypoplastic ala nasi Deep-set eyes Abn. lower eyelids Small ears
Other medical issues
 Joint hypermobility No No Yes Yes N/A No Yes
 Eye anomalies Yes No No Yes No Yes Yes
 Others No Constipation Gastroesophageal reflux Gastrostomy Conductive deafness Premature thelarche Constipation Dysphagia Gastrostomy Failure to thrive Hypotonia Flat feet Autism ADHD Delayed puberty Nasal polyps
Initial clinical suspicion Mandibulofacial dysostosis like Kabuki syndrome like Kabuki syndrome like Kabuki syndrome like Mowat Wilson like None None

Abn abnormal, ADHD attention deficit hyperactivity disorder, CNS central nervous system, DD developmental delay, HC head circumference, Het heterozygous, ID intellectual disability, IUGR intra-uterine growth retardation, LW low weight, Mi microcephaly, N within normal ranges, N/A not applicable, OW overweight, PF palpebral fissures, SD standard deviation, SS short stature.

aAt last examination.

bAccording to hg19.

cGenBank reference NM_001970.5, Ensembl reference ENST00000336458.

dUniProtKB reference P63241-1.