Weill Marchesani Syndrome

It is feasible that the major title of the record Weill Marchesani disorder is not the name you got. Kindly inspect the basic synonyms providing to discover the alternative name(s) and also condition class(s) covered by this record.


  • WMS
  • genetic mesodermal dysmorphodystrophy
  • mesodermal dysmorphodystrophy, genetic
  • spherophakia-brachymorphia disorder
  • WM disorder

Problem Subdivisions

  • None

General Discussion
Weill Marchesani disorder is an unusual hereditary problem of connective cells defined by problems of the lens of the eye, brief stature, an uncommonly brief, wide head (brachycephaly) as well as joint tightness. Weill Marchesani disorder adheres to autosomal recessive or autosomal leading inheritance.

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