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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- Genetics Home Reference: Langer-Giedion Syndrome Provides information on this condition, the genetic changes involved, how it is inherited and other sources of information.
- Trichorhinophalangeal Syndrome Type II; TRPS2 Technical information on this disorder, also known as Langer-Giedion syndrome, from the database of Online Mendelian Inheritance in Man.