Skeletal dysplasia-epilepsy-short stature syndrome

Orpha code: 1858OMIM code: 601187

Definicja

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.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Gurrieri-Sammito-Bellussi syndrome
Zespół Gurrieri, Sammito i Bellussi
Kod ORPHA
1858
Kod OMIM
601187
Kod ICD10
Q87.5
Kod ICD11
LD24.8Y

No additional description.

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