Синдром скелетної дисплазії-епілепсії-низького зросту
ORPHA:1858· ICD-10 Q87.5· Skeletal dysplasia-epilepsy-short stature syndrome
Визначення(English summary)
A rare, genetic dysostosis malformation syndrome characterized by skeletal dysplasia (rabbit ear-shaped iliac alae, delayed bone age, abnormalities of the vertebral bodies and schisis of the vertebral arches), seizures, short stature, cerebral atrophy and moderate to severe intellectual disability. Additional variable manifestations include corneal and retinal abnormalities, cataract, prognathism, dental malocclusion, brachydactyly, clinodactily, slight generalized hypotonia and hyper extensible joints.
- Поширеність
- <1 / 1 000 000
- Вік початку
- Neonatal