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Синдром летальної артеріопатії, зумовлений дефіцитом фібуліну-4

ORPHA:314718· ICD-10 Q28.8· Lethal arteriopathy syndrome due to fibulin-4 deficiency

Визначення(English summary)

A rare, genetic, vascular disorder characterized by severe aneurysmal dilatation, elongation, and tortuosity of the thoracic aorta, its branches and pulmonary arteries with stenosis at various typical locations, typically resulting in infantile demise. Variable associated features may include cutis laxa, long philtrum with thin vermillion border, hypertelorism, sagging cheeks, arachnodactyly, joint laxity and pectus deformities.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal recessive
Вік початку
Infancy, Neonatal