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. 2014 Dec 14;15:133. doi: 10.1186/s12881-014-0133-2

Table 1.

Clinical features of patients with AP4M1 mutations in this and previous studies

Parameters Present study Verkerk et al. [ 16 ] Tüysüz et al. [ 15 ]
Ind IV:3 Ind IV:4
Gender M M 3F/2M 3F/1M
Age at last examination (y.) 14 12 1.5/21/22/23/24 2.5/10.5/11/17
Head circumference −2SD −2SD −1 to −2.5 SD −2 to −4 SD
Height (cm) 157 137 NA NA
Intellectual disability Severe Severe Severe in 5/5 Severe in 3/4
Seizures + - - +
Shy character - - + +
Aggressive behavior + + - -
Stereotype laughter - - + +
Severe speech disorder + + + +
Infantile hypotonia + + + +
Hypertonia + + + +
Hyperreflexia + + NA NA
Babinski sign + + + NA
Spasticity + + + +
Club feet - - + +
Independent walking (y.) 2 4 - +/−
Ambulation - - - -
Craniofacial features
Facial hypotonia - - NA +
Bitemporal narrowing - - NA +
Broad nasal bridge - - NA +
Bulbous nose - + NA +
Short philtrum + + NA +
Brain MR imaging Yes No 3/5 4/4
Widened lateral ventricles + + +
Thin splenium of the CC + + +
Cerebellar hypoplasia/atrophy + 2/3 -

Abbreviations: + present, absent, SD standard deviation, M male, F female, NA: no data available, CC: corpus callosum, y.: years.