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Published in: Journal of Genetic Counseling 5/2008

01-10-2008 | Original Research

Genetic Counseling in Southern Iran: Consanguinity and Reason for Referral

Authors: Mohsen Fathzadeh, Mohammad Ali Babaie Bigi, Masood Bazrgar, Majid Yavarian, Hamid Reza Tabatabaee, Seyed Mohammad Akrami

Published in: Journal of Genetic Counseling | Issue 5/2008

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Abstract

Population based genetic counseling that promotes public health goals is an appropriate health care service. The genetic counseling center in Shiraz, southern Iran serves most of the clients in the region. During a 4-year period, 2,686 couples presented for genetic counseling. Data files revealed that 85% had consanguineous relationships (1.5% double first cousin, 74% first cousin, 8% second cousin, 1.5% beyond second cousin). Most prevalent reasons for referral were premarital counseling (80%), with 89% consanguinity, followed by preconception (12%), postnatal (7%), and prenatal counseling (1%). The most common abnormalities in probands or relatives were intellectual and developmental disabilities, hearing loss/impairment, and neuromuscular dystrophies. Family history of medical problem(s) and/or consanguinity was the main indication for referral in nearly every family. Premarital consanguinity poses unique challenges and opportunities. There is considerable opportunity for genetic counseling and education for couples in this population. The tradition of consanguinity, which is likely to persist in Iran, requires multidisciplinary agreement regarding the appropriate process of genetic counseling. Effective genetic counseling in Iran hinges on inclusion of data from genetic counseling services in national genomic and epidemiologic research programs.
Literature
go back to reference Abbasi-Shavazi, M. J., McDonald, P., & Chavoshi, M. H. (2006). Modernization and cultural practice of consanguineous marriage: A study of four province of Iran. European population conference: Population challenges in ageing societies, 21–24 June, Liverpool. Abbasi-Shavazi, M. J., McDonald, P., & Chavoshi, M. H. (2006). Modernization and cultural practice of consanguineous marriage: A study of four province of Iran. European population conference: Population challenges in ageing societies, 21–24 June, Liverpool.
go back to reference Akbari, M. T., Papiha, S. S., Roberts, D. F., & Farhud, D. D. (1986). Genetic differentiation among Iranian Christian communities. American Journal of Human Genetics, 38(1), 84–98.PubMed Akbari, M. T., Papiha, S. S., Roberts, D. F., & Farhud, D. D. (1986). Genetic differentiation among Iranian Christian communities. American Journal of Human Genetics, 38(1), 84–98.PubMed
go back to reference Akrami, S. M., & Osati, Z. (2007). Is consanguineous marriage religiously encouraged? Islamic and Iranian considerations. Journal of Biosocial Science, 39(2), 313–314.PubMedCrossRef Akrami, S. M., & Osati, Z. (2007). Is consanguineous marriage religiously encouraged? Islamic and Iranian considerations. Journal of Biosocial Science, 39(2), 313–314.PubMedCrossRef
go back to reference Al-Aqeel, A. I. (2005). Ethical guidelines in genetics and genomics. An Islamic perspective. Saudi Medical Journal, 26(12), 1862–1870.PubMed Al-Aqeel, A. I. (2005). Ethical guidelines in genetics and genomics. An Islamic perspective. Saudi Medical Journal, 26(12), 1862–1870.PubMed
go back to reference Al Aqeel, A. I. (2007). Islamic ethical framework for research into and prevention of genetic diseases. Nature Genetics, 39(11), 1293–1298.PubMedCrossRef Al Aqeel, A. I. (2007). Islamic ethical framework for research into and prevention of genetic diseases. Nature Genetics, 39(11), 1293–1298.PubMedCrossRef
go back to reference Al-Gazali, L. (2005). Attitudes toward genetic counseling in the United Arab Emirates. Community Genetics, 8(1), 48–51.PubMedCrossRef Al-Gazali, L. (2005). Attitudes toward genetic counseling in the United Arab Emirates. Community Genetics, 8(1), 48–51.PubMedCrossRef
go back to reference Amirshahi, P., Sunderland, E., Farhud, D. D., Tavakoli, S. H., Daneshmand, P., & Papiha, S. S. (1989). Serum proteins and erythrocyte enzymes of populations in Iran. Human Heredity, 39(2), 75–80.PubMedCrossRef Amirshahi, P., Sunderland, E., Farhud, D. D., Tavakoli, S. H., Daneshmand, P., & Papiha, S. S. (1989). Serum proteins and erythrocyte enzymes of populations in Iran. Human Heredity, 39(2), 75–80.PubMedCrossRef
go back to reference Bazregar, M., Karimi, M., Fathzadeh, M., Senemar, S., Peiravian, F., Shojaee, A., et al. (2007). Apolipoprotein E polymorphism in Southern Iran: E4 allele in the lowest reported amounts. Molecular Biology Reports, in press. DOI 10.1007/s11033-007-9113-3 Bazregar, M., Karimi, M., Fathzadeh, M., Senemar, S., Peiravian, F., Shojaee, A., et al. (2007). Apolipoprotein E polymorphism in Southern Iran: E4 allele in the lowest reported amounts. Molecular Biology Reports, in press. DOI 10.​1007/​s11033-007-9113-3
go back to reference Bittles, A. H. (2001). Consanguinity and its relevance to clinical genetics. Clinical Genetics, 60, 89–98.PubMedCrossRef Bittles, A. H. (2001). Consanguinity and its relevance to clinical genetics. Clinical Genetics, 60, 89–98.PubMedCrossRef
go back to reference Bittles, A. H. (2005). Endogamy, consanguinity and community disease profiles. Community Genetics, 8, 17–20.PubMedCrossRef Bittles, A. H. (2005). Endogamy, consanguinity and community disease profiles. Community Genetics, 8, 17–20.PubMedCrossRef
go back to reference Cotton, R. G., (2006) Human variome project, Appelbe, W., Auerbach, A. D., Becker, K., Bodmer, W., Boone, D. J., et al. (2007). Recommendations of the 2006 Human Variome Project meeting. Nature Genetics, 39(4), 433–436. Cotton, R. G., (2006) Human variome project, Appelbe, W., Auerbach, A. D., Becker, K., Bodmer, W., Boone, D. J., et al. (2007). Recommendations of the 2006 Human Variome Project meeting. Nature Genetics, 39(4), 433–436.
go back to reference Fathzadeh, M., Seyenda, Y., Khazali, H., Sheidai, M., & Farhud, D. D. (2005). Epidemiological study of T4, T3, and TSH mean concentrations in four Iranian populations. Iranian Journal of Public Health, 34(1), 74–79. Fathzadeh, M., Seyenda, Y., Khazali, H., Sheidai, M., & Farhud, D. D. (2005). Epidemiological study of T4, T3, and TSH mean concentrations in four Iranian populations. Iranian Journal of Public Health, 34(1), 74–79.
go back to reference Ghiasvand, N. M., Shirzad, E., Naghavi, M., & Vaez Movahedi, M. R. (1998). High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NRCNA) in an Iranian founding population. American Journal of Medical Genetics, 78(3), 226–232.PubMedCrossRef Ghiasvand, N. M., Shirzad, E., Naghavi, M., & Vaez Movahedi, M. R. (1998). High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NRCNA) in an Iranian founding population. American Journal of Medical Genetics, 78(3), 226–232.PubMedCrossRef
go back to reference Grant, J. C., & Bittles, A. H. (1997). The comparative role of consanguinity in infant and childhood mortality in Pakistan. Annals of Human Genetics, 61, 143–149.PubMedCrossRef Grant, J. C., & Bittles, A. H. (1997). The comparative role of consanguinity in infant and childhood mortality in Pakistan. Annals of Human Genetics, 61, 143–149.PubMedCrossRef
go back to reference Haddow, J. E. (2005). Couple screening to avoid thalassemia: Successful in Iran and instructive for us all. Journal of Medical Screening, 12, 55–56.PubMedCrossRef Haddow, J. E. (2005). Couple screening to avoid thalassemia: Successful in Iran and instructive for us all. Journal of Medical Screening, 12, 55–56.PubMedCrossRef
go back to reference Hussain, R. (1998). The role of consanguinity and inbreeding as a determinant of spontaneous abortion in Karachi, Pakistan. Annals of Human Genetics, 62(Pt 2), 147–157.PubMedCrossRef Hussain, R. (1998). The role of consanguinity and inbreeding as a determinant of spontaneous abortion in Karachi, Pakistan. Annals of Human Genetics, 62(Pt 2), 147–157.PubMedCrossRef
go back to reference Hussain, R. (1999). Community perception of reasons for preference for consanguineous marriage in Pakistan. Journal of Biosocial Science, 31, 449–461.PubMedCrossRef Hussain, R. (1999). Community perception of reasons for preference for consanguineous marriage in Pakistan. Journal of Biosocial Science, 31, 449–461.PubMedCrossRef
go back to reference Kunstmann, E., & Epplen, J. T. (2006). Genetic counseling for the public. Community Genetics, 9, 62–66.PubMedCrossRef Kunstmann, E., & Epplen, J. T. (2006). Genetic counseling for the public. Community Genetics, 9, 62–66.PubMedCrossRef
go back to reference Mannucci, P. M., Duga, S., & Peyvandi, F. (2004). Recessively inherited coagulation disorders. Blood, 104, 1243–1252.PubMedCrossRef Mannucci, P. M., Duga, S., & Peyvandi, F. (2004). Recessively inherited coagulation disorders. Blood, 104, 1243–1252.PubMedCrossRef
go back to reference Mirdehghan, S. A., Dehghan, M. H., Mohammadpour, M., Heidari, K., & Khosravi, M. (2005). Causes of sever visual impairment and blindness in schools for visually handicapped children in Iran. British Journal of Ophthalmology, 89(5), 612–614.PubMedCrossRef Mirdehghan, S. A., Dehghan, M. H., Mohammadpour, M., Heidari, K., & Khosravi, M. (2005). Causes of sever visual impairment and blindness in schools for visually handicapped children in Iran. British Journal of Ophthalmology, 89(5), 612–614.PubMedCrossRef
go back to reference Najmabadi, H., Motazacker, M. M., Garshasbi, M., Kahrizi, K., Tzschach, A., Chen, W., et al. (2007). Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Human Genetics, 121(1), 43–48.PubMedCrossRef Najmabadi, H., Motazacker, M. M., Garshasbi, M., Kahrizi, K., Tzschach, A., Chen, W., et al. (2007). Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Human Genetics, 121(1), 43–48.PubMedCrossRef
go back to reference Ordookhani, A., Mirmiran, P., Hajipour, R., Hedayati, M., & Azizi, F. (2002). Screening for congenital hypothyroidism in the Islamic Republic of Iran: Strategies, obstacles and future perspectives. Eastern Mediterranean Health Journal, 8(4–5), 480–489.PubMed Ordookhani, A., Mirmiran, P., Hajipour, R., Hedayati, M., & Azizi, F. (2002). Screening for congenital hypothyroidism in the Islamic Republic of Iran: Strategies, obstacles and future perspectives. Eastern Mediterranean Health Journal, 8(4–5), 480–489.PubMed
go back to reference Reed, S. C. (1974). A short history of genetic counseling. Social Biology, 21, 332–339.PubMed Reed, S. C. (1974). A short history of genetic counseling. Social Biology, 21, 332–339.PubMed
go back to reference Resta, R. G. (2006). Defining and redefining the scope and goal of genetic counseling. American Journal of Medical Genetics, 142c, 269–275.PubMedCrossRef Resta, R. G. (2006). Defining and redefining the scope and goal of genetic counseling. American Journal of Medical Genetics, 142c, 269–275.PubMedCrossRef
go back to reference Resta, R. G., Biesecker, B. B., Bennett, R. L., Blum, S., Hahn, S. E., Strecker, M. N., et al. (2006b). A new definition of genetic counseling: National Society of Genetic Counselors’ task force report. Journal of Genetic Counseling, 15, 77–83.PubMedCrossRef Resta, R. G., Biesecker, B. B., Bennett, R. L., Blum, S., Hahn, S. E., Strecker, M. N., et al. (2006b). A new definition of genetic counseling: National Society of Genetic Counselors’ task force report. Journal of Genetic Counseling, 15, 77–83.PubMedCrossRef
go back to reference Rezaei, N., Pourpak, Z., Aghamohammadi, A., Farhoudi, A., Movahedi, M., Gharagozlou, M., et al. (2006). Consanguinity in primary immunodeficiency disorders; the report from Iranian Primary Immunodeficiency Registry. American Journal of Reproductive Immunology, 56(2), 145–151.PubMedCrossRef Rezaei, N., Pourpak, Z., Aghamohammadi, A., Farhoudi, A., Movahedi, M., Gharagozlou, M., et al. (2006). Consanguinity in primary immunodeficiency disorders; the report from Iranian Primary Immunodeficiency Registry. American Journal of Reproductive Immunology, 56(2), 145–151.PubMedCrossRef
go back to reference Saadat, M., Ansari-Lari, M., & Farhud, D. D. (2004). Consanguineous marriage in Iran. Annals of Human Biology, 31(2), 263–269.PubMedCrossRef Saadat, M., Ansari-Lari, M., & Farhud, D. D. (2004). Consanguineous marriage in Iran. Annals of Human Biology, 31(2), 263–269.PubMedCrossRef
go back to reference Samavat, A., & Modell, B. (2004). Iranian national thalassaemia screening programme. Builders Merchants Journal, 329(7475), 1134–1137. Samavat, A., & Modell, B. (2004). Iranian national thalassaemia screening programme. Builders Merchants Journal, 329(7475), 1134–1137.
go back to reference Senemar, S., Fathzadeh, M., Ganjbakhsh, A. H., Bazrgar, M., Tarami, B., & Babaie Bigi, M. (2007). Epidemiological and clinical assessment of PKU babies in the National Screening Program of Newborn in Fars province. Iranian Journal of Pediatrics, 17(Suppl 3), 6. Senemar, S., Fathzadeh, M., Ganjbakhsh, A. H., Bazrgar, M., Tarami, B., & Babaie Bigi, M. (2007). Epidemiological and clinical assessment of PKU babies in the National Screening Program of Newborn in Fars province. Iranian Journal of Pediatrics, 17(Suppl 3), 6.
go back to reference Walter, H., Farhud, D. D., Danker-Hopfe, H., & Amirshahi, P. (1991). Investigations on the ethnic variability of the ABO blood group polymorphism in Iran. Zeitschrift fuÉr Morphologie und Anthropologie, 78(3), 289–306. Walter, H., Farhud, D. D., Danker-Hopfe, H., & Amirshahi, P. (1991). Investigations on the ethnic variability of the ABO blood group polymorphism in Iran. Zeitschrift fuÉr Morphologie und Anthropologie, 78(3), 289–306.
go back to reference Zakzouk, S. (2002). Consanguinity and hearing impairment in developing countries: A custom to be discouraged. Journal of Laryngology and Otology, 116(10), 811–816.PubMed Zakzouk, S. (2002). Consanguinity and hearing impairment in developing countries: A custom to be discouraged. Journal of Laryngology and Otology, 116(10), 811–816.PubMed
go back to reference Zlotogora, J. (1997a). Genetic disorders among Palestinian Arab; 1. Effect of consanguinity. American Journal of Medical Genetics, 68, 472–475.PubMedCrossRef Zlotogora, J. (1997a). Genetic disorders among Palestinian Arab; 1. Effect of consanguinity. American Journal of Medical Genetics, 68, 472–475.PubMedCrossRef
go back to reference Zlotogora, J. (1997b). Genetic disorders among Palestinian Arab; 2. Hydrocephalus and neural tube defects. American Journal of Medical Genetics, 71, 33–35.PubMedCrossRef Zlotogora, J. (1997b). Genetic disorders among Palestinian Arab; 2. Hydrocephalus and neural tube defects. American Journal of Medical Genetics, 71, 33–35.PubMedCrossRef
go back to reference Zlotogora, J. (2007). Multiple mutations responsible for frequent genetic diseases in isolated populations. European Journal of Human Genetics, 15(3), 272–278.PubMedCrossRef Zlotogora, J. (2007). Multiple mutations responsible for frequent genetic diseases in isolated populations. European Journal of Human Genetics, 15(3), 272–278.PubMedCrossRef
go back to reference Zlotogora, J., Barges, S., Bisharat, B., & Shalev, S. A. (2006). Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community. American Journal of Medical Genetics, 140(15), 1644–1646.PubMed Zlotogora, J., Barges, S., Bisharat, B., & Shalev, S. A. (2006). Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community. American Journal of Medical Genetics, 140(15), 1644–1646.PubMed
Metadata
Title
Genetic Counseling in Southern Iran: Consanguinity and Reason for Referral
Authors
Mohsen Fathzadeh
Mohammad Ali Babaie Bigi
Masood Bazrgar
Majid Yavarian
Hamid Reza Tabatabaee
Seyed Mohammad Akrami
Publication date
01-10-2008
Publisher
Springer US
Published in
Journal of Genetic Counseling / Issue 5/2008
Print ISSN: 1059-7700
Electronic ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-008-9163-2

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