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Tibia vara in a patient with Bardet-Biedl syndrome
N E Motzkin1, A J Bianco, D Zimmerman
1Department of Orthopedics and Metabolism, Mayo Clinic, Rochester, MN 55905.
Mayo Clinic Proceedings
|June 11, 1992
Abstract:
The Bardet-Biedl syndrome is characterized by polydactyly, hypogonadism, obesity, mental retardation, and retinitis pigmentosa. Several other skeletal findings include hip dysplasia, short stature, and skull deformities. The patient described in this report has the classic findings of Bardet-Biedl syndrome in conjunction with tibia vara and irregular physes of the lower extremities.
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