Keutel syndrome

Last revised by Rohit Sharma on 12 Jul 2021

Keutel syndrome is an extremely rare inherited condition.

It is characterized by:

Occurs as a result of matrix γ-carboxyglutamate protein (MGP) mutations. 

It is thought to carry a pattern of autosomal recessive inheritance.

It was first described by J Keutel in 1971 2.

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