Consanguinity in primary immunodeficiency disorders; the report from Iranian primary immunodeficiency registry

American Journal of Reproductive Immunology

Volumn 56, Issue 2, 2006, Pages 145-151

  Rezaei, Nima ^a   Pourpak, Zahra ^a   Aghamohammadi, Asghar ^a   Farhoudi, Abolhassan ^a   Movahedi, Masoud ^a   Gharagozlou, Mohammad ^a   MirSaeid Ghazi, Bahram ^a   Atarod, Lida ^a   Abolmaali, Kamran ^a   Mahmoudi, Maryam ^a   Mansouri, Davoud ^b   Arshi, Saba ^c   Tarash, Naser Javaher ^c   Sherkat, Roya ^d   Amin, Reza ^e   Kashef, Sara ^e   Hosseini, Reza Farid ^f   Mohammadzadeh, Iraj ^g   Shabestari, Mehrnaz Sadeghi ^h   Nabavi, Mohammad ⁱ   Moin, Mostafa ^a   more..

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d ISFAHAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^e SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^f MASHHAD UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^g BABOL UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^h TABRIZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

ⁱ SEMNAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Consanguinity; Family history; Iran; Primary immunodeficiency disorders

Indexed keywords

CD4 ANTIGEN; IMMUNOGLOBULIN G;

ADOLESCENT; ADULT; AGED; ARTICLE; ATAXIA TELANGIECTASIA; AUTOSOMAL RECESSIVE INHERITANCE; CELLULAR IMMUNODEFICIENCY; CHEDIAK HIGASHI SYNDROME; CHILD; CHRONIC GRANULOMATOUS DISEASE; COMBINED IMMUNODEFICIENCY; CONSANGUINITY; CONTROLLED STUDY; FEMALE; GENETIC COUNSELING; GENETIC RISK; HUMAN; HUMORAL IMMUNE DEFICIENCY; IMMUNE DEFICIENCY; IMMUNOGLOBULIN G DEFICIENCY; INCIDENCE; INFANT; IRAN; MAJOR CLINICAL STUDY; MALE; PHYLOGENETIC TREE; PRIORITY JOURNAL; REGISTER; REPRODUCTIVE HEALTH; RISK ASSESSMENT; RISK FACTOR;

ADOLESCENT; ADULT; CHILD; CONSANGUINITY; FEMALE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; IRAN; MALE; PEDIGREE; REGISTRIES;

EID: 33745747405     PISSN: 10467408     EISSN: 16000897     Source Type: Journal    
DOI: 10.1111/j.1600-0897.2006.00409.x     Document Type: Article

References (27)

1. Aghamohammadi A, Moein M, Farhoudi A, Pourpak Z, Rezaei N, Abolmaali K, Movahedi M, Gharagozlou M, Ghazi BM, Mahmoudi M, Mansouri D, Arshi S, Trash NJ, Akbari H, Sherkat R, Hosayni RF, Hashemzadeh A, Mohammadzadeh I, Amin R, Kashef S, Alborzi A, Karimi A, Khazaei H: Primary immunodeficiency in Iran: First report of national registry of PID in children and adults. J Clin Immunol 2002; 22: 375-380.
2. Notarangelo L, Casanova JL, Fischer A, Puck J, Rosen F, Seger R, Geha R; International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee: Primary immunodeficiency diseases: An update. J Allergy Clin Immunol 2004; 114: 677-687.
3. Bonilla FA, Geha RS: Primary immunodeficiency diseases. J Allergy Clin Immunol 2003; 111: S571-S851.
4. al-Attas RA, Rahi AH: Primary anFibody deficiency in Arabs: first report from eastern Saudi Arabia. J Clin Immunol 1998; 18: 368-371.
5. Javier FC 3rd, Moore CM, Sorensen RU: Distribution of primary immunodeficiency diseases diagnosed in a pediatric tertiary hospital. Ann Allergy Asthma Immunol 2000; 84: 25-30.
6. Matamoros Flori N, Mila Llambi J, Espanol Boren T, Raga Borja S, Fontan Casariego G: Primary immunodeficiency Fyndrome in Spain: first report of the National Registry in Children and Adults. J Clin Immunol 1997; 17: 333 -339.
7. Zelazko M, Carneiro-Sampaio M, Cornejo de Luigi M, Garcia de Olarte D, Porras Madrigal O, Berron Perez R, Cabello A, Rostan MV, Sorensen RU: Primary immunodeficiency diseases in Latin America: First report from eight countries participating in the LAGID. Latin American Group for Primary Immunodeficiency Diseases. J Clin Immunol 1998; 18: 161-166.
8. Stiehm ER, Ochs HG, Winkelstein JA: Immunologic disorders: general consideration. In Immunologic Disorders in Infants and Children, ER Stiehm, HD Ochs, JA Winkelstein (eds). USA, Elsevier Saunders, 2005, pp 289-355.
9. Bittles A: Consanguinity and its relevance to clinical genetics. Clin Genet 2001; 60: 89-98.
10. Saadat M, Ansari-Lari M, Farhud DD: Consanguineous marriage in Iran. Ann Hum Biol 2004; 31: 263-269.
11. Bittles AH: The role and significance of consanguinity as a demographic variable. Pop Dev Rev 1994; 20: 561-584.
12. Bener A, Abdulrazzaq YM, al-Gazali LI, Micallef R, al-Khayat AI, Gaber T: Consanguinity and associated socio-demographic factors in the United Arab Emirates. Hum Hered 1996; 46: 256-264.
13. Jurdi R, Saxena PC: The prevalence and correlates of consanguineous marriages in Yemen: Similarities and contrasts with other Arab countries. J Biosoc Sci 2003; 35: 1-13.
14. Khlat M: Consanguineous marriaTes in Beirut: time trends, spatial distribution. Soc Biol 1988; 35: 324-330.
15. Hafez M, El-Tahan H, Awadalla M, El-Khayat H, Abdel-Gafar A, Ghoneim M: Consanguineous matings in the Egyptian population. J Med Genet 1983; 20: 58-60.
16. Jaber L, Halpern GJ, Shohat M: The impact of consanguinity worldwide. Community Genet 1998; 1: 12-17.
17. Rezaei N, Farhoudi A, Pourpak Z, Aghamohammadi A, Moin M, Movahedi M, Gharagozlou M: Neutropenia in Iranian patients with primary immunodeficiency disorders. Haematologica 2005; 90: 554-556.
18. Givens BP, Hirschman C: Modernization and consanguineous marriage in Iran. J Marriage Fam 1994; 56: 820-834.
19. Plum M: Computation of inbreeding and relationship coefficients. J Hered 1954; 45: 92-94.
20. Bittles AH, Mason WM, Greene J, Rao NA: Reproductive behavior and health in consanguineous marriages. Science 1991; 252: 789-794.
21. Hasui M: Chronic granulomatous disease in Japan: Incidence and natural history. The study group of phagocyte disorders of Japan. Pediatr Int 1999; 41: 589-593.
22. Winkelstein JA, Marino MC, Johnston RB Jr, Boyle J, Curnutte J, Gallin JI, Malech HL, Holland SM, Ochs H, Quie P, Buckley RH, Foster CB, Chanock SJ, Dickler H: Chronic granulomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 2000; 79: 155-169.
23. Movahedi M, Aghamohammadi A, Rezaei N, Shahnavaz N, Jandaghi AB, Farhoudi A, Pourpak Z, Moin M, Gharagozlou M, Mansouri D: Chronic granulomatous disease: A clinical survey of 41 patients from the Iranian primary immunodeficiency registry. Int Arch Allergy Immunol 2004; 134: 253 -259.
24. Bradburd D: The ruTes and the game: the practice of marriage among the Komachi. Am Ethnologist 1984; 11: 738-753.
25. Albar MA: Ethical considerations in the prevention and management of genetic disorders with special emphasis on religious considerations. Saudi Med J 2002; 23: 627-632.
26. Alwan A, Modell B: Community Control of Genetic and Congenital Disorders. EMRO Technical Publication Series 24. Alexandria, Egypt: WHO Regional Office for the Eastern Mediterranean, 51 pp.
27. Tabori U, Mark Z, Amariglio N, Etzioni A, Golan H, Biloray B, Toren A, Rechavi G, Dalal I: Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome. Clin Genet 2004; 65: 322-326.