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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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Provides clinical information on this disorder including the case study of a 12 year old girl. [PDF]
Technical information on this disorder, also known as Langer-Giedion syndrome, from the database of Online Mendelian Inheritance in Man.
Technical information on this disorder, also known as Langer-Giedion syndrome, from the database of Online Mendelian Inheritance in Man.
Provides clinical information on this disorder including the case study of a 12 year old girl. [PDF]
Last update:
March 5, 2021 at 6:25:12 UTC
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