Skip to main content
Erschienen in: Journal of Immigrant and Minority Health 3/2010

01.06.2010 | Brief Communication

Birth Defects and Genetic Disorders Among Arab Americans—Michigan, 1992–2003

verfasst von: Emad A. Yanni, Glenn Copeland, Richard S. Olney

Erschienen in: Journal of Immigrant and Minority Health | Ausgabe 3/2010

Einloggen, um Zugang zu erhalten

Abstract

Birth defects and genetic disorders are leading causes of infant morbidity and mortality in many countries. Population-based data on birth defects among Arab-American children have not been documented previously. Michigan has the second largest Arab-American community in the United States after California. Using data from the Michigan Birth Defects Registry (MBDR), which includes information on parents’ country of birth and ancestry, birth prevalences were estimated in offspring of Michigan women of Arab ancestry for 21 major categories of birth defects and 12 congenital endocrine, metabolic, and hereditary disorders. Compared with other non-Hispanic white children in Michigan, Arab-American children had similar or lower birth prevalences of the selected types of structural birth defects, with higher rates of certain hereditary blood disorders and three categories of metabolic disorders. These estimates are important for planning preconception and antenatal health care, genetic counseling, and clinical care for Arab Americans.
Literatur
1.
Zurück zum Zitat Carmichael SL, Shaw GM, Kaidarova Z. Congenital malformations in offspring of Hispanic and African-American women in California, 1989–1997. Birth Defects Res A, Clin Mol Teratol. 2004;70(6):382–8. doi:10.1002/bdra.20012.CrossRef Carmichael SL, Shaw GM, Kaidarova Z. Congenital malformations in offspring of Hispanic and African-American women in California, 1989–1997. Birth Defects Res A, Clin Mol Teratol. 2004;70(6):382–8. doi:10.​1002/​bdra.​20012.CrossRef
2.
Zurück zum Zitat Christianson A, Howson C, Modell B. Executive summary March of dimes global report on birth defects. White Plains, NY: March of Dimes Birth Defects Foundation; 2006. March of Dimes. Christianson A, Howson C, Modell B. Executive summary March of dimes global report on birth defects. White Plains, NY: March of Dimes Birth Defects Foundation; 2006. March of Dimes.
4.
Zurück zum Zitat Brittingham A, De la Cruz CP. We the people of Arab ancestry in the United States, Census 2000 special reports. US Census Bureau; 2005 Jan 3. Report No: 36. Brittingham A, De la Cruz CP. We the people of Arab ancestry in the United States, Census 2000 special reports. US Census Bureau; 2005 Jan 3. Report No: 36.
6.
Zurück zum Zitat Canfield MA, Honein MA, Yuskiv N, Xing J, Mai CT, Collins JS, et al. National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999–2001. Birth Defects Res A, Clin Mol Teratol. 2006;76(11):747–56. doi:10.1002/bdra.20294.CrossRef Canfield MA, Honein MA, Yuskiv N, Xing J, Mai CT, Collins JS, et al. National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999–2001. Birth Defects Res A, Clin Mol Teratol. 2006;76(11):747–56. doi:10.​1002/​bdra.​20294.CrossRef
7.
Zurück zum Zitat Hoodfar E, Teebi A. Genetic referrals of Middle Eastern origin in a western city: inbreeding and disease profile. J Med Genet. 1996;33(3):212–5.CrossRefPubMed Hoodfar E, Teebi A. Genetic referrals of Middle Eastern origin in a western city: inbreeding and disease profile. J Med Genet. 1996;33(3):212–5.CrossRefPubMed
8.
Zurück zum Zitat Korman SH. Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3–1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic status. Mol Genet Metab. 2004;82(2):121–9. doi:10.1016/j.ymgme.2004.03.002.CrossRefPubMed Korman SH. Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3–1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic status. Mol Genet Metab. 2004;82(2):121–9. doi:10.​1016/​j.​ymgme.​2004.​03.​002.CrossRefPubMed
11.
Zurück zum Zitat William CA, Hauser KW, Correia JA, Frias JL. Ascertainment of gastroschisis using the ICD-9-CM surgical procedure code. Birth Defects Res Clin Mol Teratol. 2005;73(10):646–8. doi:10.1002/bdra.20205.CrossRef William CA, Hauser KW, Correia JA, Frias JL. Ascertainment of gastroschisis using the ICD-9-CM surgical procedure code. Birth Defects Res Clin Mol Teratol. 2005;73(10):646–8. doi:10.​1002/​bdra.​20205.CrossRef
Metadaten
Titel
Birth Defects and Genetic Disorders Among Arab Americans—Michigan, 1992–2003
verfasst von
Emad A. Yanni
Glenn Copeland
Richard S. Olney
Publikationsdatum
01.06.2010
Verlag
Springer US
Erschienen in
Journal of Immigrant and Minority Health / Ausgabe 3/2010
Print ISSN: 1557-1912
Elektronische ISSN: 1557-1920
DOI
https://doi.org/10.1007/s10903-008-9203-x

Weitere Artikel der Ausgabe 3/2010

Journal of Immigrant and Minority Health 3/2010 Zur Ausgabe