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Homocystinuria A REPORT OF TWO CASES AND REVIEW OF THE LITERATURE
RODNEY K. BEALS
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From the Crippled Children's Division and Division of Orthopedic Surgery, University of Oregon Medical School, Portland
1969 by The Journal of Bone and Joint Surgery, Incorporated
The Journal of Bone & Joint Surgery.  1969; 51:1564-1572 
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Abstract

Homocystiniuria is an inborn error of amino acid metabolism that produces generalized abnormalities which are not discernible at birth but which appear during growth and development.

Early diagnosis is of benefit to the family and probably to the affected individual; and, although no single physical abnormality is diagnostic of the disease, a simple urine test is available which will detect this amino acid disorder.

Orthopaedists should be alert to the possibility of homocystinuria in children with mental retardation, eye abnormalities, thromboembolic disease, seizures, scoliosis, genu valgum, cavus or flat feet, characteristic facies, osteoporosis, multiple fractures, or psychological disorders.

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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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