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

More general terms

• genetic syndrome (multisystem disorder)

Database

• OMIM: https://mirror.omim.org/entry/245150