Hands and feet in the Apert syndrome
- 22 May 1995
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 57 (1) , 82-96
- https://doi.org/10.1002/ajmg.1320570119
Abstract
We studied 44 pairs of hands and 37 pairs of feet in Apert syndrome, utilizing clinical, dermatoglyphic, and radiographic methods. We also studied histologic sections of the hand from a 31-week stillborn fetus. Topic headings discussed include: clinical classification of syndactyly; correlations between types of hands and feet in the same patient; dermatoglyphics; anatomy of the hand; radiologic assessment; comparison with other studies; histologic assessment of the hand; acrocephalosyndactyly vs. acrocephalopoly-syndactyly: a pseudodistinction; and some generalizations.Keywords
This publication has 44 references indexed in Scilit:
- Localization of craniosynostosis Adelaide type to 4p16Human Molecular Genetics, 1995
- Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3Nature Genetics, 1995
- Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.Journal of Medical Genetics, 1994
- Genetic Heterogeneity among Craniosynostosis Syndromes: Mapping the Saethre-Chotzen Syndrome Locus between D7S513 and D7S516 and Exclusion of Jackson-Weiss and Crouzon Syndrome Loci from 7pGenomics, 1994
- Skeletal abnormalities in the Apert syndromeAmerican Journal of Medical Genetics, 1993
- Visceral anomalies in the Apert syndromeAmerican Journal of Medical Genetics, 1993
- Upper and lower airway compromise in the apert syndromeAmerican Journal of Medical Genetics, 1992
- Apparent Apert syndrome with polydactyly: Rare pleiotropic manifestation or new syndrome?American Journal of Medical Genetics, 1987
- Deformities of the Great Toe in Apert??s SyndromePublished by Wolters Kluwer Health ,1981
- Apert's syndrome (a type of acrocephalosyndactyly)–observations on a British series of thirty‐nine cases*Annals of Human Genetics, 1959