Langer-Giedion syndrome (Q46620): Difference between revisions
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Revision as of 15:19, 13 August 2026
Langer-Giedion syndrome or trichorhinophalangeal syndrome type 2 is a chromosomal anomaly syndrome characterised by the association of intellectual deficit and numerous other anomalies including redundant skin, multiple cartilaginous exostoses, characteristic facies and cone-shaped phalangeal epiphyses.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD24.80 |
||
| English | Langer-Giedion syndrome |
Langer-Giedion syndrome or trichorhinophalangeal syndrome type 2 is a chromosomal anomaly syndrome characterised by the association of intellectual deficit and numerous other anomalies including redundant skin, multiple cartilaginous exostoses, characteristic facies and cone-shaped phalangeal epiphyses. |
