Спадкова нейрошкірна вада розвитку
ORPHA:1062· ICD-10 D18.0· Hereditary neurocutaneous malformation
Визначення(English summary)
A rare genetic vascular anomaly characterized by the presence of angiomatous lesions affecting the skin, brain, and spinal cord. Lesions of the central nervous system have a marked tendency to bleed. There have been no further descriptions in the literature since 1988.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal dominant
- Вік початку
- Childhood, Infancy