Langer-Giedion syndrome (Q46620): Difference between revisions
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A síndrome de Langer-Giedon ou síndrome tricorrinofalangiana tipo 2 é uma síndrome de anomalia cromossômica caracterizada pela associação de déficit intelectual e inúmeras outras anomalias, incluindo pele redundante, múltiplas exostoses cartilaginosas, fácies características e epífises falangianas em forma de cone. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
