An aetiological classification of birth defects for epidemiological research
Open Access
- 1 January 2005
- journal article
- medical genetics-in-practice
- Published by BMJ in Journal of Medical Genetics
- Vol. 42 (1) , 54-57
- https://doi.org/10.1136/jmg.2004.023309
Abstract
Background: Congenital anomaly registers collect data on antenatally and postnatally detected anomalies for surveillance, research, and public health purposes. Each anomaly is coded using the International Statistical Classification of Diseases and Related Health Problems (ICD-9/ICD-10) based on body systems, allowing accurate comparisons between registers for individual anomalies. When commencing an environmental, epidemiological study, it became clear to us that there is no standard classification that takes aetiology into account. This paper describes a new classification for use in studies addressing aetiology. Method: A classification system was evolved and piloted using cases in a study of geographical variation in congenital anomaly prevalence.1 Cases that were difficult to categorise were noted, and after discussion with a team of experts, the classification was adjusted accordingly. Results and conclusion: A robust, hierarchical method of classifying birth defects into eight categories has been produced, for use at source of data registration in conjunction with, but independent of, ICD coding.Keywords
This publication has 11 references indexed in Scilit:
- Evidence for Selective Advantage of Pathogenic FGFR2 Mutations in the Male Germ LineScience, 2003
- Rare congenital disorders, imprinted genes, and assisted reproductive technologyThe Lancet, 2003
- Guidelines for case classification for the national birth defects prevention studyBirth Defects Research Part A: Clinical and Molecular Teratology, 2003
- Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19American Journal of Human Genetics, 2003
- Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting DefectsAmerican Journal of Human Genetics, 2002
- Exclusive paternal origin of new mutations in Apert syndromeNature Genetics, 1996
- On the parental origin of de novo mutation in man.Journal of Medical Genetics, 1991
- Population surveillance of sentinel anolaliesMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1989
- SPONTANEOUS MUTATION AND PARENTAL AGE IN HUMANS1987
- A Developmental Approach to the Classification of Birth DefectsAnnals of Plastic Surgery, 1985