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Schaaf-Yang syndrome

ORPHA:398069· ICD-10 Q87.1

Definition

A rare imprinting disorder characterized by muscular hypotonia, joint contractures/arthrogryposis, developmental delay, usually mild to moderate intellectual disability, short stature, hypogonadism, autism spectrum disorder and, less often, hyperphagia and seizures.

Prevalence
<1 / 1 000 000
Inheritance
Not applicable
Age of onset
Antenatal, Neonatal