Arterial dissection-lentiginosis syndrome

Orpha code: 1682OMIM code: 600459

Definition

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
Classification

Malformation syndrome

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

No additional description.

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