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Bilateral femoral dysgenesis with micrognathia, cleft palate, anomalies of the spine and pelvis, and foot deformities. Clinical and radiological findings.

作者信息

Burck U, Riebel T, Held K R, Stoeckenius M

出版信息

Helv Paediatr Acta. 1981 Nov;36(5):473-82.

PMID:7309536
Abstract

Two girls afflicted with bilateral femoral hypoplasia, micrognathia, cleft palate, anomalies of the spine and pelvis, and foot deformities are reported. Based on 10 cases reported in the literature the following points are emphasized: 1. Femoral hypoplasia may be bilateral or unilateral. 2. Many patients show asymmetrical changes. 3. To our knowledge, the complete syndrome including a cleft palate has been reported only in females. 4. Femoral hypoplasia without a cleft palate may represent a different entity, of possibly autosomal dominant inheritance, or may occur in children of diabetic mothers.

摘要

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引用本文的文献

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The femoral hypoplasia-unusual facies syndrome.股骨发育不全-特殊面容综合征
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