Langer-Giedion Syndrome
"Langer-Giedion Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses. INTELLECTUAL DISABILITY and abnormalities of chromosome 8 are often present. The exostoses in this syndrome appear identical to those of hereditary multiple exostoses (EXOSTOSES, HEREDITARY MULTIPLE).
Descriptor ID |
D015826
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MeSH Number(s) |
C05.116.099.708.582
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Concept/Terms |
Langer-Giedion Syndrome- Langer-Giedion Syndrome
- Langer Giedion Syndrome
- Syndrome, Langer-Giedion
- Giedion-Langer Syndrome
- Giedion Langer Syndrome
- Syndrome, Giedion-Langer
- Trichorhinophalangeal Syndrome Type II
- Trichorhinophalangeal Syndrome Type 2
- Trichorhinophalangeal Syndrome, Type II
- Tricho-Rhino-Phalangeal Syndrome Type II
- Tricho Rhino Phalangeal Syndrome Type II
- TRPSII
- Acrodysplasia V
- Acrodysplasia Vs
- Trichorhinophalangeal Syndrome with Exostoses
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Below are MeSH descriptors whose meaning is more general than "Langer-Giedion Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Langer-Giedion Syndrome".
This graph shows the total number of publications written about "Langer-Giedion Syndrome" by people in this website by year, and whether "Langer-Giedion Syndrome" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2012 | 1 | 0 | 1 | 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Langer-Giedion Syndrome" by people in Profiles.
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Armour CM, Smith A, Hartley T, Chardon JW, Sawyer S, Schwartzentruber J, Hennekam R, Majewski J, Bulman DE, Suri M, Boycott KM. Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events. Am J Med Genet A. 2016 07; 170(7):1820-5.
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Snyder JR, Berk DR, Kwan A, Hudgins L, Bruckner AL. What is your diagnosis? Trichorhinophalangeal syndrome type I. Cutis. 2012 Feb; 89(2):56, 73-4.
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