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]
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- Recently edited by merlin1
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