Skeletal dysplasia-epilepsy-short stature syndrome

Orpha code: 1858OMIM code: 601187

Definition

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
Classification

Malformation syndrome

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

No additional description.

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