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