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Apert's hand

Overview page. Subjects: Plastic and Reconstructive Surgery.

See Apert’s syndrome. All involved portions of upper limb have skeletal unions, incomplete joint segmentation and incomplete separation of rays. All hands have skeletal...

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Apert's hand

Overview page. Subjects: Plastic and Reconstructive Surgery.

See Apert’s syndrome. All involved portions of upper limb have skeletal unions, incomplete joint segmentation and incomplete separation of rays. All hands have skeletal...

See overview in Oxford Index

Apert’s hand

Andrew Hodges.

in A-Z of Plastic Surgery

January 2008; p ublished online January 2009 .

Reference Entry. Subjects: Plastic and Reconstructive Surgery. 528 words.

See Apert’s syndrome. • All involved portions of upper limb have skeletal unions, incomplete joint segmentation and incomplete separation

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Upton classification

Andrew Hodges.

in A-Z of Plastic Surgery

January 2008; p ublished online January 2009 .

Reference Entry. Subjects: Plastic and Reconstructive Surgery. 5 words.

See Apert’s hands.

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Apert’s syndrome

Andrew Hodges.

in A-Z of Plastic Surgery

January 2008; p ublished online January 2009 .

Reference Entry. Subjects: Plastic and Reconstructive Surgery. 230 words.

Acrocephalosyndactyly with bicoronal synostosis, Midface hypoplasia, cleft palate, and complex syndactyly. See Apert’s hand. • Most are sporadic, but

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acrocephalosyndactyly

Overview page. Subjects: Medicine and Health.

n. any one of a group of related inherited disorders, including Apert syndrome, resulting in abnormalities of the skull (craniosynostosis), face, and hands and feet...

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Apert's syndrome

John Lackie.

in A Dictionary of Biomedicine

January 2010; p ublished online January 2010 .

Reference Entry. Subjects: Clinical Medicine. 38 words.

A developmental disorder (Apert–Crouzon disease) characterized by craniosynostosis (premature closure of skull sutures), midface hypoplasia, and syndactyly of the hands

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Acrosyndactyly

Overview page. Subjects: Plastic and Reconstructive Surgery.

One of the Congenital hand anomalies. Fusion of digits distally. Mainly sporadic, non-hereditary occurrence. Associated with Constriction ring syndrome. Bilateral in 50%,...

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Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of <i>FGFR2</i>

Michael Oldridge, Peter W. Lunt, Elaine H. Zackai, Donna M. McDonald-McGinn, Maximilian Muenke, Dominique M. Moloney, Stephen R. F. Twigg, John K. Heath, Timothy D. Howard, George Hoganson, Deborah M. Gagnon, Ethylin Wang Jabs and Andrew O. M. Wilkie.

in Human Molecular Genetics

January 1997; p ublished online January 1997 .

Journal Article. Subjects: Genetics and Genomics. 5014 words.

Dominantly acting, allelic mutations of the fibroblast growth factor receptor 2 (FGFR2) gene have been described in five craniosynostosis syndromes. In Apert syndrome, characterised by...

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