Morgagni-Stewart-Morel syndrome

Orpha code: 77296OMIM code: 144800

Definicja

A rare cranial malformation characterized by hyperostosis frontalis interna, variably associated with metabolic and endocrine disorders (such as obesity, diabetes mellitus, and hirsutism, among others). Compression by calvarial thickening may lead to cerebral atrophy and present with cognitive impairment, neuropsychiatric symptoms, headaches, and epilepsy. The condition predominantly affects women.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
Hyperostosis frontalis interna
Hiperostoza czołowa wewnętrzna
Kod ORPHA
77296
Kod OMIM
144800
Kod ICD10
M85.2
Kod ICD11
FB80.3

No additional description.

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