Langer-Giedion syndrome is a condition that causes bone abnormalities and distinctive facial features. People with this condition have multiple ...
Langer-Giedion Syndrome (LGS), also called trichorhinophalangeal syndrome type II (TRPS2) or LGCR (for "Langer-Giedion Chromosome Region"),   is a very uncommon ...
Langer-Giedion syndrome (LGS) is a very rare genetic disorder that is characterized by distinct facial features and bone abnormalities, including thinly-growing hair ...
Langer Giedion Syndrome symptoms, causes, diagnosis, and treatment information for Langer Giedion Syndrome (Trichorhinophalangeal syndrome type 2) with alternative ...
Learn about Langer-Giedion Syndrome, its symptoms, genetic testing, diagnosis, genetic inheritance and treatment or patient management of this condition.
Langer-Giedion syndrome - associated with the TRPS1 gene. The deletion or mutation of the TRPS1 gene and at least one other gene on chromosome 8 causes ...
Trichorhinophalangeal syndrome type 2 (TRPS2), also known as Langer-Giedion syndrome, is an extremely rare inherited multisystem disorder. The condition is ...
Langer-Giedion syndrome (LGS) is a very rare genetic disorder that is characterized by distinct facial features and bone abnormalities, including thinly ...
Learn about Langer Giedion Syndrome from patients' first hand experiences and trusted online health resources, including common treatments and medications. 14 ...
Summary. Langer-Giedon syndrome or trichorhinophalangeal syndrome type 2 is characterized by the association of intellectual deficit and numerous other anomalies ...