Синдром Груббена-де Кока-Боргграфа
ORPHA:2101· ICD-10 Q87.8· Grubben-de Cock-Borghgraef syndrome
Визначення(English summary)
Grubben-de Cock-Borghgraef syndrome is a rare intellectual disability syndrome characterized by pre- and postnatal growth deficiency, generalized muscular hypotonia, developmental delay (particularly of speech and language), hypotrophy of distal extremities, small and puffy hands and feet, eczematous skin and dental anomalies (i.e. small, widely-spaced teeth). Partial agenesis of the corpus callosum and a selective immunoglobulin IgG2 subclass deficiency have also been reported in some patients.
- Поширеність
- <1 / 1 000 000
- Вік початку
- Antenatal, Neonatal