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Інтелектуальна недостатність, тип Бірк-Бареля

ORPHA:166108· ICD-10 Q87.8· Birk-Barel syndrome

Визначення(English summary)

Intellectual disability, Birk-Barel type is a rare, genetic, syndromic intellectual disability characterized by congenital central hypotonia, developmental delay, moderate to severe intellectual disability and subtle dysmorphic features which evolve over time (dolichocephaly, myopathic facies, ptosis, short and broad philtrum, tented upper lip vermillion, palatal anomalies, mild micro- and/or retrognathia). Patients present reduced facial movements, lethargy, weak cry, transient neonatal hypoglycemia, severe feeding difficulties and failure to thrive. Dysphagia, particularly of solid food, asthenic body build, joint contractures and scoliosis are additional features.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant
Вік початку
Infancy