Orphanet: Autosomal dominant cutis laxa
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Autosomal dominant cutis laxa

Disease definition

A rare connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated in some cases with internal organ involvement.

ORPHA:90348

Classification level: Disorder
  • Synonym(s):
    • ADCL
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q82.8
  • OMIM: 123700  614434  616603
  • UMLS: C0268350
  • MeSH: -
  • GARD: 1639
  • MedDRA: -

Detailed information

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