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Issue title: Pediatric Limb Deficiency
Article type: Research Article
Authors: Kasperski, Stefanie B. | Wilson, R. Douglas
Affiliations: The Center for Fetal Diagnosis and Treatment at the Children's Hospital of Philadelphia, PA, USA | Department of Obstetrics and Gynecology, University of Calgary, Canada
Note: [] Address for correspondence: Stefanie B. Kasperski, Center for Fetal Diagnosis and Treatment, 34th Street and Civic Center Boulevard, Philadelphia, PA 19104-4399, USA. Tel.: +1 800 IN UTERO; Fax: +1 (215) 590 2447; E-mail: [email protected]
Abstract: Congenital limb deficiencies/hypoplasias are a heterogeneous group of anomalies that range from mild abnormalities of little long-term clinical significance to the severe limb-reduction defects spectrum associated with fetal thalidomide exposure. This article reviews the approach to the prenatal evaluation of congenital limb deficiency/hypoplasia and provides an overview of selected limb reduction defects along with a discussion of etiology and genetic aspects. A case report detailing the prenatal evaluation of a fetus with a skeletal dysplasia illustrates the importance of a comprehensive, multidisciplinary and dysmorphology-based approach.
Keywords: Limb difference, genetics, skeletal dysplasia, prenatal diagnosis
DOI: 10.3233/PRM-2009-0080
Journal: Journal of Pediatric Rehabilitation Medicine, vol. 2, no. 3, pp. 189-193, 2009
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