Description of the disease * EnglishPolish Pobierz sekcję do PDF 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 - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl