Laurence–Moon syndrome

Laurence–Moon syndrome
Boy with Laurence-Moon syndrome
SpecialtyMedical genetics 

Laurence–Moon syndrome (LMS) is a rare autosomal recessive[1] genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities.[2]

  1. ^ Farag, T. I.; Teebi, A. H. W. S. (Feb 1988). "Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population". Clinical Genetics. 33 (2): 78–82. doi:10.1111/j.1399-0004.1988.tb03414.x. PMID 3359670. S2CID 43584088.
  2. ^ "Laurence-Moon Syndrome | Doctor | Patient". Patient. 24 February 2015. Retrieved 13 December 2016.
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