Directory of Langer-Giedion Syndrome Resources

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Langer-Giedion syndrome is a rare autosomal dominant genetic disorder caused by a deletion of chromosomal material. Associated features include learning difficulties, short stature, distinctive facial features, small head and skeletal abnormalities

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• Support Groups

Resources in This Category

• Genetics Home Reference: Langer-Giedion Syndrome

  http://ghr.nlm.nih.gov/condition/langer-giedion-syndrome
  Provides information on this condition, the genetic changes involved, how it is inherited and other sources of information.

• Indian Pediatrics: Langer-Giedion Syndrome

  http://www.indianpediatrics.net/feb2006/174.pdf
  Provides clinical information on this disorder including the case study of a 12 year old girl.

• Trichorhinophalangeal Syndrome Type II; TRPS2

  http://omim.org/entry/150230
  Technical information on this disorder, also known as Langer-Giedion syndrome, from the database of Online Mendelian Inheritance in Man.

 

Home > Health > Conditions and Diseases > Genetic Disorders > Langer-Giedion Syndrome

 

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