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Arterial dissection-lentiginosis syndrome
Disease 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).
ORPHA:1682
Classification level: Disorder- Synonym(s): -
- Prevalence: <1 / 1 000 000
- Inheritance: Unknown
- Age of onset: Childhood
- ICD-10: Q87.8
- OMIM: 600459
- UMLS: C1838122
- MeSH: -
- GARD: -
- MedDRA: -
A summary on this disease is available in Deutsch (2004) Español (2015) Italiano (2015) Nederlands (2015) Français (2005)
Detailed information
Guidelines
- Clinical practice guidelines
- Deutsch (2013) - AWMF


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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