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Arthrogryposis-ectodermal dysplasia syndrome

Disease definition

A rare, genetic developmental defect during embryogenesis syndrome characterized by camptodactyly, joint contractures with amyotrophy, and ectodermal anomalies (oligodontia, enamel abnormalities, longitudinally broken nails, hypohidrotic skin with tendency to excessive bruising and scarring after injuries and scratching), as well as growth retardation, kyphoscoliosis, mild facial dysmorphism, and microcephaly. There have been no further descriptions in the literature since 1992.

ORPHA:3200

Classification level: Disorder
  • Synonym(s):
    • Stoll-Alembik-Finck syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Unknown 
  • Age of onset: Infancy, Neonatal
  • ICD-10: -
  • OMIM: 601701
  • UMLS: C1866427
  • MeSH: -
  • GARD: 5029
  • MedDRA: -

Additional information

Further information on this disease

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