Синдром Морганї-Стюарта-Мореля
ORPHA:77296· ICD-10 M85.2· Morgagni-Stewart-Morel syndrome
Визначення(English summary)
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.
- Поширеність
- Unknown
- Успадкування
- Autosomal dominant, X-linked recessive
- Вік початку
- Adult