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  5. Langer-Giedion Syndrome  3 Sites
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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Indian Pediatrics: Langer-Giedion Syndrome - Provides clinical information on this disorder including the case study of a 12 year old girl. 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.
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