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Stiff skin syndrome

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Description

Stiff skin syndrome is characterized by hard, thick skin, usually over the entire body, which limits joint mobility and causes flexion contractures. Other occasional findings include lipodystrophy and muscle weakness (Loeys et al., 2010). Patients with similar phenotypes involving stiff skin have been described; see, e.g., familial progressive scleroderma (181750), symmetric lipomatosis (151800), and congenital fascial dystrophy (228020).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

283

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Genes

External Links

  • OMIM

    184900

  • Orphanet

    2833

  • HPO
  • Medgen

    C1861456

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