Cutis laxa

Orpha code: 209OMIM code:

Definicja

Cutis laxa (CL) is an inherited or acquired connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated with skeletal and developmental anomalies and, in some cases, with severe systemic involvement. Several different forms of inherited CL have been described, differentiated on the basis of the mode of inheritance and differences in the extent of internal organ involvement, associated anomalies and disease severity.

Disease data
Klasyfikacja

Clinical group

Kod ORPHA
209
Kod OMIM
-
Kod ICD10
Q82.8
Kod ICD11
EE41.0

No additional description.

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