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Stargardt disease 4

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Description

Stargardt disease is the most common hereditary macular dystrophy and is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. STGD is most commonly inherited as an autosomal recessive trait (see 248200), but STGD4 is inherited as an autosomal dominant trait (summary by Kniazeva et al., 1999).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

112

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Genes

External Links

  • OMIM

    603786

  • Orphanet
  • HPO
  • Medgen

    C1863534

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