Description of the disease * EnglishPolish Pobierz sekcję do PDF 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 - *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