Langer-Giedion syndrome (Q46620): Difference between revisions

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@@ Property / Collection date: 13 August 2026 / rank @@
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Latest 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.