Keutel syndrome (Q94167): Difference between revisions
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Síndrome de Keutel é uma síndrome de anomalia de desenvolvimento autossômica recessiva caracterizada por calcificação difusa da cartilagem, braquitelefalangismo, estenoses de artéria pulmonar periférica e dismorfismo facial. | |||
| description / en | description / en | ||
Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism. | |||
Revision as of 09:17, 16 August 2026
Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1083151379 |
||
| English | Keutel syndrome |
Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism. |
