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Keutel syndrome
Genetics:
- autosomal recessive
- associated with defects in matrix Gla protein (MGP)
Clinical manifestations:
- abnormal cartilage calcification
- peripheral pulmonary stenosis
- sensorineural hearing loss
- midfacial hypoplasia
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 245150
References
OMIM :accession 245150