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
Genetics Home Reference: 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
Provides clinical information on this disorder including the case study of a 12 year old girl. [PDF]
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.
Last update:March 21, 2015 at 21:36:32 UTC