Apert Syndrome: orthopedic treatment

被引：0

作者：

Lopez Lopez, Daniel ^{[1
]}

Alonso Tajes, Francisco ^{[1
]}

Rosende Bautista, Carolina ^{[1
]}

Lopez Lopez, Luis ^{[1
]}

机构：

[1] Univ A Coruna, Dept Ciencias Saude, Podol EU Enfermaria & Podoloxia, C Nat Seoane,Esquina San Ramon S-N, La Coruna 15403, Spain

来源：

REVISTA INTERNACIONAL DE CIENCIAS PODOLOGICAS | 2011年 / 5卷 / 01期

关键词：

Acrocephalosyndactyly Type I; Craniosynostosis; Syndactyly; Apert Syndrome;

D O I：

10.5209/rev_RICP.2011.v5.n1.19429

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Apert syndrome is an autosomal dominant disorder characterized by craniosynostosis, midfacial malformations and symmetric syndactyly of hands and feet. We present a case of a female Caucasian, 45 years old, prenatal diagnosis at 24 weeks gestation, apert syndrome type I, after sonography showing features deformity were observed characteristics. She refered pain at the first head of the first metatarsal of the left foot, long evolution that improves with rest and with the intake of oral analgesics, which is the realization of orthopedic treatment palie that the disease process.

引用

页码：29 / 35

页数：7

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