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Langer-Giedion Syndrome
(Acrodysplasia V; Giedion-Langer Syndrome; Trichorhinophalangeal Syndrome Type II)
Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses. mental retardation and abnormalities of chromosome 8 are often present. The exostoses in this syndrome appear identical to those of hereditary multiple exostoses (exostoses, HEREDITARY MULTIPLE).
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 of Langer-Giedion syndrome en.wikipedia.org |  File:Langer-Giedion syndrome. commons.wikimedia.org |  (Langer-Giedion Syndrome) dermatology.cdlib.org |  (Langer-Giedion Syndrome) dermatology.cdlib.org |
 Langer-Giedion syndrome, www.wellsphere.com |  Ben has Langer-Giedion www.wellsphere.com |  Langer Giedion syndrome - “The radiopaedia.org |  (Langer-Giedion Syndrome) radiopaedia.org |
Diagnosis and therapies
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Wikipedia
Langer-Giedion syndrome, Langer–Giedion syndrome, Tricho–rhino–phalangeal syndrome, Osteochondrodysplasia, Tricho-rhino-phalangeal syndrome Type 1, Hereditary multiple exostosesPotocki-Shaffer syndrome, Buccal exostosis, Subungual exostosis, Jan Sophus Jansen,
More information
- Reported cases - Summary of cases reported on this disease.
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