Gómez-López-Hernández syndrome

Orpha code: 1532OMIM code: 601853

Definition

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
Classification

Malformation syndrome

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

No additional description.

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