
Roger E. Stevenson (ed.)
et al.
Published:
01 October 2015
Online ISBN:
9780199386055
Print ISBN:
9780199386031
Contents
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Introduction Introduction
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Anatomical Embryology Anatomical Embryology
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Molecular Embryology Molecular Embryology
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Classification and Terminology Classification and Terminology
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References References
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2.1 Polydactyly 2.1 Polydactyly
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2.1A Preaxial Polydactyly 2.1A Preaxial Polydactyly
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.1B Postaxial Polydactyly 2.1B Postaxial Polydactyly
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.1C Mesoaxial Polydactyly 2.1C Mesoaxial Polydactyly
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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References References
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References References
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References References
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2.2 Syndactlyly 2.2 Syndactlyly
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2.2A Syndactyly Type I 2.2A Syndactyly Type I
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2B Syndactyly Type II 2.2B Syndactyly Type II
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2C Syndactyly Type III 2.2C Syndactyly Type III
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2D Syndactyly Type IV 2.2D Syndactyly Type IV
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2E Syndactyly Type V 2.2E Syndactyly Type V
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2F Complete Syndactyly 2.2F Complete Syndactyly
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2G Cenani-Lenz Syndactyly 2.2G Cenani-Lenz Syndactyly
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.2H Symbrachydactyly 2.2H Symbrachydactyly
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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References References
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References References
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References References
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References References
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References References
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References References
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References References
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References References
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2.3 Brachydactyly 2.3 Brachydactyly
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2.3A Brachydactyly Type A1 2.3A Brachydactyly Type A1
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.3B Brachydactyly Type A2 2.3B Brachydactyly Type A2
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.3C Brachydactyly Type A3 2.3C Brachydactyly Type A3
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.3D Brachydactyly Type B 2.3D Brachydactyly Type B
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.3E Brachydactyly Type C 2.3E Brachydactyly Type C
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.3F Brachydactyly Type D 2.3F Brachydactyly Type D
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.3G Brachydactyly Type E 2.3G Brachydactyly Type E
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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References References
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References References
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2.4 Osseous Deficiencies of the Hands and Feet 2.4 Osseous Deficiencies of the Hands and Feet
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2.4A Preaxial Deficiency 2.4A Preaxial Deficiency
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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2.4B Postaxial Deficiency 2.4B Postaxial Deficiency
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Definition: Definition:
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Treatment: Treatment:
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Prognosis: Prognosis:
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References References
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References References
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2.5 Terminal Transverse Deficiency 2.5 Terminal Transverse Deficiency
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References References
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2.6 Split-Hand/Foot Malformation 2.6 Split-Hand/Foot Malformation
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References References
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2.7 Macrodactyly 2.7 Macrodactyly
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References References
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2.8 Camptodactyly 2.8 Camptodactyly
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References References
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2.9 Clubfoot 2.9 Clubfoot
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References References
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Cite
Everman, David B., 'Hands and Feet', in Roger E. Stevenson, and others (eds), Human Malformations and Related Anomalies, 3 edn, Oxford Monographs on Medical Genetics (New York , 2015; online edn, Oxford Academic, 1 Oct. 2015), https://doi.org/10.1093/med/9780199386031.003.0002, accessed 4 May 2025.
Abstract
Malformations of the hands and feet are common and are usually easily visualized and recognized immediately. These malformations include reduction defects and extra or malformed digits, and may affect the skeletal, soft tissue, or both elements. They may be functionally and cosmetically significant and are often associated with other malformations or as part of recognizable syndromes. There are numerous genetic and nongenetic causes.
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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct.
Readers must therefore always …
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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct.
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