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Bowen Hutterite Syndrome

Abstract

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Synonyms of Bowen Hutterite Syndrome

  • Bowen-Conradi Hutterite Syndrome
  • Bowen-Conradi Syndrome
  • Hutterite Syndrome, Bowen-Conradi Type

Disorder Subdivisions

  • No subdivisions found.

General Discussion

Bowen Hutterite syndrome is a rare genetic disorder that is apparent at birth (congenital). The disorder is characterized by growth delays before birth (intrauterine growth retardation); failure to grow and gain weight at the expected rate (failure to thrive) during infancy; malformations of the head and facial (craniofacial) area, resulting in a distinctive appearance; and other physical abnormalities. These may include restricted joint movements, abnormal deviation (clinodactyly) or permanent flexion (camptodactyly) of the fifth fingers, foot deformities, and/or undescended testes (cryptorchidism) in affected males. Some affected infants may also have kidney (renal), brain, and/or other malformations. Bowen Hutterite syndrome is inherited as an autosomal recessive trait.

Bowen Hutterite Syndrome Resources

Organizations:

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