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. 2021 Aug 10;2(4):100049. doi: 10.1016/j.xhgg.2021.100049

Table 2.

Phenotypes, genotypes, and demographic features of individuals with an AHDC1 missense mutation

Patient ID 1 3 5 6 7 8 9 10
Mutation

Nucleotide change c.139C>T c.1610G>A c.1646G>A c.1819G>A c.2374G>C c.4042T>C c. 4370A>G c.4432C>T
Protein change p.Pro47Ser p.Gly537Asp p.Arg549His p.Asp607Asn p.Gly792Arg p.Ser1348Pro p.Asp1457Gly p.Pro1478Ser
Age 14 years 10 years 6 years 23 years 12 years 10 years 2 years 11 years
Sex M F F M F M F F
Ethnicity white African American/white white white white white NA Latino/Hispanic

Growth

Stature (percentile) <10th 99th >90th 43rd 99th 30th 1st 1st
Scoliosis Y N N N N N NA N

Comprehensive skills and language

M-CHAT score 4 NA NA 15 4 NA 0
Autism diagnosis Y N N Y N Y NA Y
Current languagea 3 3 2 3 3 0 1 1
Age at first word 11 months 3 years ~2 years 2.5 years 2 years NA NA 2–3 years
Age using two words together ~2 years ~4 years ~12–13 years not recalled NA NA
Age at following command 2 years NA NA has trouble following command not reported NA 1.5 years

Mobility

Hypotonia diagnosis Y N N Y Y Y Y Y
Independent walking Y Y Y Y walking with support Y Y
Age at independent walking ~2 years 11 months 15 months 1.5 years 2 years 1 year

Sleep/airway

Sleep apnea N Y N N N N
Using breathing support N Y (CPAP at night) N N N N

Neurology

MRI normal NA not done abnormal abnormal abnormal abnormal abnormal
EEG normal NA NA NA normal NA abnormal normal
Seizure Y Y NA Y Y Y Y N
Age at first seizure 3 years NA 22 years 2–3 years 6 years 3 days NA
Ataxia N N N Y Y Y

Vision

Wearing glasses or contacts N Y N N Y Y N N
Visual acuity 20/30 hyperopia, night blindness normal NA NA hypermetropia hypermetropia NA
Strabismus N N N N N Y Y N

Dysmorphic features

Features coarse facial features long palpebral fissures, deep-set eyes, hypertelorism, macrocephaly, cleft palate broad forehead, thin upper lip macrocephaly (likely familial) upslanted palpebral fissures, microcephaly, low-set ears broad forehead, wide nasal bridge, brachycephaly, microtia, clinodactyly 5th finger, mild microcephaly almond-shaped eyes, thin upper lip, brachycephaly, microcephaly, protuberant ears upslanting palpebral fissures, microcephaly

Of the total of 10 individuals, five joined the XGS Registry and provided all available clinical data (individuals 1, 3, 6, 7, and 10). Partial data were available for three of the additional five known individuals (5, 8, 9). M-CHAT, Modified Checklist for Autism in Toddlers; CPAP, continuous positive airway pressure; MRI, magnetic resonance imaging; EEG, electroencephalogram; M, male; F, female; Y, yes; N, no; NA, not applicable.

a

Current language: 0, no words; 1, <50 words; 2, no sentence but >50 words; and 3, full sentence >200 words.