Catel–Manzke syndrome (Q5051865)
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Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis
- Catel-Manzke Syndrome
- Palatodigital syndrome, Catel-Manzke type
- Pierre Robin sequence-hyperphalangy-clinodactyly syndrome
- Micrognathia digital syndrome
- Palatodigital syndrome Catel-Manzke type
- Pierre Robin Syndrome With Hyperphalangy and Clinodactyly
- Catel Manzke syndrome
- CATMANS
- Index Finger Anomaly With Pierre Robin Syndrome
- Hyperphalangy-Clinodactyly of Index Finger With Pierre Robin Syndrome
- Pierre Robin syndrome-hyperphalangy-clinodactyly syndrome
- CATEL-MANZKE SYNDROME; CATMANS
- Index finger anomaly-Pierre Robin syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Catel–Manzke syndrome |
Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis |
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Sitelinks
Wikipedia(5 entries)
- dewiki Catel-Manzke-Syndrom
- enwiki Catel–Manzke syndrome
- itwiki Sindrome di Catel-Manzke
- plwiki Zespół Catela-Manzkego
- trwiki Catel-Manzke sendromu