Arterial dissection-lentiginosis syndrome

Orpha code: 1682OMIM code: 600459

Definicja

A rare association syndrome, reported in several members of two families to date, characterized by arterial dissection, occurring at an early age and presenting with a range of manifestations depending on the vascular territory involved (ex. headache, dysphasia, hemiparesis), in association with cystic medial necrosis and multiple lentigines (brown and black in color and mainly affecting the skin of the trunk and extremities).

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
1682
Kod OMIM
600459
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

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