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Laurence-Moon syndrome : ウィキペディア英語版
Laurence–Moon syndrome

Laurence–Moon syndrome (LMS) is a rare autosomal recessive genetic disorder associated with retinitis pigmentosa, extra digits, spastic paraplegia, hypogonadism and mental retardation.
== Genetics ==

LMS is inherited in an autosomal recessive manner.〔 This means the defective gene responsible for the disorder is located on an autosome, and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Laurence–Moon syndrome」の詳細全文を読む



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