Gómez-López-Hernández syndrome

Orpha code: 1532OMIM code: 601853

Definicja

A rare neurocutaneous syndrome characterized by the association of cerebellum (rhombencephalosynapsis), cranial nerves (trigeminal anesthesia), and scalp (alopecia) abnormalities. Other features observed in patients were craniosynostosis, midfacial hypoplasia, bilateral corneal opacities, low-set ears, short stature, moderate intellectual impairment and ataxia. Hyperactivity, depression, self-injurious behaviour and bipolar disorder have also been reported.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Cerebellotrigeminal-dermal dysplasia syndrome
Dysplazja móżdżkowo-trójdzielno-skórna
Kraniosynostoza - łysienie - defekt mózgu
Craniosynostosis-alopecia-brain defect syndrome
Kod ORPHA
1532
Kod OMIM
601853
Kod ICD10
Q07.8
Kod ICD11
-

No additional description.

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