Limb defects associated with major congenital anomalies: Clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems
Autor: | Giuseppe Zampino, J D Erickson, Claude Stoll, Martina C. Cornel, Richard S. Olney, Paul Merlob, Annukka Ritvanen, Osvaldo M. Mutchinick, Lorenzo D. Botto, E. E. Castilla, M. L. Martínez-Frías, Muin J. Khoury, Pierpaolo Mastroiacovo, Guido Cocchi, J. Goujard, Aldo Rosano |
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Rok vydání: | 2000 |
Předmět: |
VASCULAR PATHOGENESIS
etiology prevalence Population Encephalocele Dysgenesis limb abnormalities Medicine MALFORMATIONS education international registry POPULATION Genetics (clinical) Multiple abnormalities education.field_of_study Omphalocele ABNORMALITIES business.industry Gastroschisis Microtia REDUCTION DEFECTS Anatomy medicine.disease DEFICIENCY Atresia epidemiology multiple abnormalities business |
Zdroj: | American Journal of Medical Genetics, 93(2), 110-116. WILEY-LISS |
ISSN: | 1096-8628 0148-7299 |
DOI: | 10.1002/1096-8628(20000717)93:2<110::aid-ajmg6>3.0.co;2-9 |
Popis: | Although limb defects associated with other congenital anomalies are rarely studied, they may provide insights into limb development that may be useful for etiologic studies and public health monitoring, me pooled data from II birth defect registries that are part of the International Clearinghouse for Birth Defects Monitoring Systems. We identified 666 infants, born from 1983 through 1993, who had a non-syndromal limb defect plus at least one other major malformation (rate 12.9/100,000 population). We used observed/expected ratios and log-linear models to detect association patterns. We found that specific limb defects occurred with relatively distinct sets of malformations. Preaxial limb defects occurred more frequently with microtia, esophageal atresia, anorectal atresia, heart defects, unilateral kidney dysgenesis, and some axial skeleton defects; postaxial defects with hypospadias; transverse defects with craniofacial defects, micrognathia, ring constrictions, and muscular defects; intercalary defects with omphalocele; split hand/foot with encephalocele; and amelia with anorectal atresia, omphalocele, severe genitalia defects, unilateral kidney dysgenesis, gastroschisis, and ring constriction. Log-linear modeling identified higher order associations among some of these same malformations. (C) 2000 Wiley-Liss, Inc. |
Databáze: | OpenAIRE |
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