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STAR syndrome

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This is an old revision of this page, as edited by Alillich (talk | contribs) at 18:53, 17 April 2018 (Updated citation to GARD and added epidemiology information. #citeNLM2018). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

STAR syndrome

STAR syndrome is a rare X-linked dominant disorder. Its core features include toe syndactyly, telecanthus and anogenital and renal malformations.[1] The underlying cause is mutation in the FAM58A gene. There have currently been 10 cases reported.[2]

References

  1. ^ "Entry # 300707". OMIM. November 3, 2017.
  2. ^ "STAR syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2018-04-17.

External links

Retrieved from "https://en.wikipedia.org/w/index.php?title=STAR_syndrome&oldid=836936282"