Catel-Manzke syndrome (Q94135): Difference between revisions
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Síndrome de Catel-Manzke é uma associação rara que combina micrognatia, glossoptose e fenda palatina (sequência de Pierre Robin) com uma anomalia de ambos os dedos indicadores (ossículo acessório na articulação metacarpofalangiana com desvio ulnar resultante). | |||
| description / en | description / en | ||
Catel-Manzke syndrome is a rare association combining micrognathia, glossoptosis and cleft palate (Pierre Robin sequence) with an anomaly of both index fingers (accessory ossicle at the metacarpophalangeal joint with resulting ulnar deviation). | |||
Revision as of 09:15, 16 August 2026
Catel-Manzke syndrome is a rare association combining micrognathia, glossoptosis and cleft palate (Pierre Robin sequence) with an anomaly of both index fingers (accessory ossicle at the metacarpophalangeal joint with resulting ulnar deviation).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1023183031 |
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| English | Catel-Manzke syndrome |
Catel-Manzke syndrome is a rare association combining micrognathia, glossoptosis and cleft palate (Pierre Robin sequence) with an anomaly of both index fingers (accessory ossicle at the metacarpophalangeal joint with resulting ulnar deviation). |
