Literature DB >> 20664281

Parental consanguinity and the risk of primary immunodeficiency disorders: report from the Kuwait National Primary Immunodeficiency Disorders Registry.

Waleed Al-Herz1, Kamal K Naguib, Luigi D Notarangelo, Raif S Geha, Amal Alwadaani.   

Abstract

BACKGROUND: It is proposed that consanguineous marriages increase the risk of primary immunodeficiency disorders (PID). The aim of this study is to review the frequency and pattern of parental consanguinity among PID patients and to determine its effects on the distribution of different PID, the patients' performance status and the risk of death.
METHOD: The data was obtained from the Kuwait National Primary Immunodeficiency Disorders Registry. The coefficient of inbreeding was determined for each patient and the patients' overall performance status was assessed using the Lansky Play Performance Scale and the Karnofsky Performance Scale.
RESULTS: A total of 128 patients with PID from 99 families are reported. A family history suggestive of PID and parental consanguinity was reported in 44 and 75% of the patients respectively, while the mean coefficient of inbreeding was 0.044067. There were statistically significant associations between both a family history of PID and parental consanguinity and PID category, the risk of death and the patients' overall performance status. Evidence of autosomal recessive transmission of disease was present in 44% of the patients.
CONCLUSIONS: Parental consanguinity is a risk factor for the development of PID. There is a need to increase the public awareness of the health consequences of consanguineous marriages.
Copyright © 2010 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2010        PMID: 20664281     DOI: 10.1159/000319212

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  6 in total

Review 1.  Classification of primary immunodeficiency diseases by the International Union of Immunological Societies (IUIS) Expert Committee on Primary Immunodeficiency 2011.

Authors:  H Chapel
Journal:  Clin Exp Immunol       Date:  2012-04       Impact factor: 4.330

2.  Parental consanguinity is associated with a severe phenotype in common variable immunodeficiency.

Authors:  Claire Rivoisy; Laurence Gérard; David Boutboul; Marion Malphettes; Claire Fieschi; Isabelle Durieu; François Tron; Agathe Masseau; Pierre Bordigoni; Laurent Alric; Julien Haroche; Cyrille Hoarau; Alice Bérézné; Maryvonnick Carmagnat; Gael Mouillot; Eric Oksenhendler
Journal:  J Clin Immunol       Date:  2011-10-15       Impact factor: 8.317

3.  Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait.

Authors:  Waleed Al-Herz; Raj Ragupathy; Michel J Massaad; Raja'a Al-Attiyah; Arti Nanda; Karin R Engelhardt; Bodo Grimbacher; Luigi Notarangelo; Talal Chatila; Raif S Geha
Journal:  Clin Immunol       Date:  2012-03-30       Impact factor: 3.969

4.  Survival and predictors of death among primary immunodeficient patients: a registry-based study.

Authors:  Waleed Al-Herz; Mohamed A A Moussa
Journal:  J Clin Immunol       Date:  2011-12-30       Impact factor: 8.317

5.  Major histocompatibility complex class II deficiency in Kuwait: clinical manifestations, immunological findings and molecular profile.

Authors:  Waleed Al-Herz; Osama Alsmadi; Motasem Melhem; Mike Recher; Francesco Frugoni; Luigi D Notarangelo
Journal:  J Clin Immunol       Date:  2012-11-10       Impact factor: 8.317

Review 6.  ICON: the early diagnosis of congenital immunodeficiencies.

Authors:  John Routes; Mario Abinun; Waleed Al-Herz; Jacinta Bustamante; Antonio Condino-Neto; Maria Teresa De La Morena; Amos Etzioni; Eleonora Gambineri; Elie Haddad; Lisa Kobrynski; Francoise Le Deist; Shigeaki Nonoyama; Joao Bosco Oliveira; Elena Perez; Capucine Picard; Nima Rezaei; John Sleasman; Kathleen E Sullivan; Troy Torgerson
Journal:  J Clin Immunol       Date:  2014-03-12       Impact factor: 8.542

  6 in total

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