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Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needs

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References

  • Al HH (1996) Unique demographic situation in the United Arab Emirates. Am J Med Genet 61:1

    Article  Google Scholar 

  • Al-Gazali L, Hamamy H, Al-Arrayad S (2006) Genetic disorders in the Arab world. BMJ 333(7573):831–834, Review

    Article  PubMed Central  PubMed  Google Scholar 

  • Alwan A, Modell B (1997) Community control of genetic and congenital disorders. Technical Publication Series 24. WHO: Eastern Mediterranean Regional Office, Alexandria, Egypt

    Google Scholar 

  • Bittles AH (2003) Consanguineous marriage and childhood health. Dev Med Child Neurol 45(8):571–576, Review

    Article  CAS  PubMed  Google Scholar 

  • Bundey S, Alam H (1993) A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreeding. Eur J Hum Genet 1(3):206–219

    CAS  PubMed  Google Scholar 

  • Christianson AL, Howson CP, Modell B (2006) March of Dimes Global Report on birth defects: the hidden toll of dying and disabled children. March of Dimes Birth Defects Foundation. White Plains, New York

    Google Scholar 

  • Christianson A, Zimmern R, Kristoffersson U, Schmidtke J, Kent A, Raouf R, Barreiro C, Nippert I (2013) Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations. J Community Genet 4(3):297–308

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Costello A, Tomkins A. Child heath in developing countries (1997). Medicine health issues in developing countries. Medicine pp 3–8

  • Corry PC (2002) Intellectual disability and cerebral palsy in a UK community. J Community Genet 5:201–204

    Article  CAS  Google Scholar 

  • Dawodu A, Al-Ghazali L, Varadi E, Varghese M, Nath K, Rajan V (2005) Genetic contribution to high neonatally lethal malformation rate in the United Arab Emirates. J Community Genet 8:31

    Article  CAS  Google Scholar 

  • Ministry of Health Annual Health Report (2011) Prepared by the Department of Health Information & Statistics, Directorate General of Planning, Ministry of Health, Sultanate of Oman Ministry of National Economy Statistical Data [www.mone.gov.om]. Accessed 21 Feb 2014

  • Modell B (2002) Possibilities for the control of congenital and genetic disorders in Oman. Report of WHO Consultant to Ministry of Health, Sultanate of Oman

    Google Scholar 

  • Penchaszadeh VB, Christianson AL, Glugliani R, Boulygenkov V, Katz M (1999) Services for the prevention and management of genetic disorders and birth defects in developing countries. J Community Genet 2:196–201

    Article  CAS  Google Scholar 

  • Rajab A, Patton MA (1997) Major factors determining frequencies of haemoglobinopathies in Oman. Letter to the Editor. Am J Med Genet 71:240–242

    Article  CAS  PubMed  Google Scholar 

  • Rajab A, Vaishnav A, Freeman NV, Patton MA (1998) Neural tube defects and congenital hydrocephalus in Oman. J Trop Pediatr 44:300–303

    Article  CAS  PubMed  Google Scholar 

  • Rajab A, Patton M (1999) Development and use of a national haemoglobinopathy register in Oman. Letter to the Editor. J. Community Genet 2:47–48

    Article  CAS  PubMed  Google Scholar 

  • Rajab AG, Patton MA, Modell B (2000) Study of haemoglobinopathies in Oman through a national register. Saudi Med J 21(12):1168–1172

    CAS  PubMed  Google Scholar 

  • Rajab A, Patton MA (2000) A study of consanguinity in the Sultanate of Oman. Ann Hum Biol 3:321–326

    Google Scholar 

  • Rajab A, Bappal B, Al-Shaikh H, Al-Khusaibi S, Mohammed AJ (2005) Common autosomal recessive diseases in Oman derived from a hospital-based registry. J Community Genet 8:27–30

    Article  CAS  Google Scholar 

  • Rajab A, Patton M. (2012) Genetic diseases in the Sultanate of Oman. In: Dhavendra Kumar (ed) Genomics and health in the developing world. Oxford monograph on medical genetics. Oxford University Press. Chapter 54 pp. 678–693

  • Rajab A, Al Rashdi I, Al SQ (2013) Genetic services and testing in the Sultanate of Oman. Sultanate of Oman steps into modern genetics. J Community Genet 4:391–397

    Article  PubMed Central  PubMed  Google Scholar 

  • Topley JM, Dawodu AH (1995) The pattern of congenital anomalies among UAE nationals. Saudi Med J 16:425–428

    Google Scholar 

  • Zlotogora J (2002) What is the birth defect risk associated with consanguineous marriages? Am J Med Genet 109:70–71

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

The authors would like to thank the Oman Research Council for funding the study. We thank all the Omani mothers who provided health information. The authors sincerely thank the senior officials of the Ministry of Health for their support and sincere gratitude to all Regional Health authorities and medical professionals of the Ministry of Health in the Regions of Oman contributing to the field work. The authors also thank Dr. Leo Ten Kate, and Prof. Irma Nippert for their valuable comments. The experiments performed during the study comply with the current laws of the Sultanate of Oman.

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Correspondence to A. Rajab.

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This study was funded by Oman Research Counsul.

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Rajab, A., Al Salmi, Q., Jaffer, J. et al. Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needs. J Community Genet 5, 283–289 (2014). https://doi.org/10.1007/s12687-014-0182-4

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  • DOI: https://doi.org/10.1007/s12687-014-0182-4

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