JBJS | Pyle's Disease (Familial Metaphyseal Dysplasia) A PRESENTATION OF TWO CASES AND ARGUMENT FOR ITS SEPARATION FROM CRANIOMETAPHYSEAL DYSPLASIA

The Journal of Bone & Joint Surgery, Volume 52, Issue 2

Journal Contents | March 01, 1970

Pyle's Disease (Familial Metaphyseal Dysplasia) A PRESENTATION OF TWO CASES AND ARGUMENT FOR ITS SEPARATION FROM CRANIOMETAPHYSEAL DYSPLASIA

ROBERT J. GORLIN; MICHAEL F. KOSZALKA; JÜRGEN SPRANGER

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School of Dentistry, University of Minnesota, Minneapolis, Minnesota 55455 Veterans Administration Center, Fargo, North Dakota 58102 Pediatric Clinic, University of Kiel, Kiel, Germany

1970 by The Journal of Bone and Joint Surgery, Incorporated

The Journal of Bone & Joint Surgery. 1970; 52:347-354

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Abstract

Case presentations are made of Pyle's disease in male siblings and fourteens reports of Pyle's disease from the literature are cited. The disease appears to be inherited

[See figure in the PDF file]

as an autosomal recessive trait. It is clearly distinguishable from craniometaphyseal dysplasia.

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These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.

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ROBERT J. GORLIN, MICHAEL F. KOSZALKA, JÜRGEN SPRANGER; Pyle's Disease (Familial Metaphyseal Dysplasia) A PRESENTATION OF TWO CASES AND ARGUMENT FOR ITS SEPARATION FROM CRANIOMETAPHYSEAL DYSPLASIA. The Journal of Bone & Joint Surgery. 1970 Mar;52(2):347-354.

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