Primary immunodeficiencies in highly consanguineous North African populations

Annals of the New York Academy of Sciences

Volumn 1238, Issue 1, 2011, Pages 42-52

  Barbouche, Mohamed Ridha ^a   Galal, Nermeen ^b   Ben Mustapha, Imen ^a   Jeddane, Leïla ^c   Mellouli, Fethi ^d   Ailal, Fatima ^c   Bejaoui, Mohamed ^d   Boutros, Jeanette ^b   Marsafy, Aisha ^b   Bousfiha, Ahmed Aziz ^c  

^a PASTEUR INSTITUTE OF TUNIS   (Tunisia)

^b CAIRO UNIVERSITY   (Egypt)

^c HASSAN II UNIVERSITY   (Morocco)

^d CENTRE NATIONAL DE GREFFE DE MOELLE OSSEUSE   (Tunisia)

Author keywords

Consanguinity; Immunodeficiency; North Africa; Pediatrics; Recessive

Indexed keywords

AGAMMAGLOBULINEMIA; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; AUTOSOMAL RECESSIVE DISORDER; BLOOM SYNDROME; CHEDIAK HIGASHI SYNDROME; CHRONIC GRANULOMATOUS DISEASE; COMMON VARIABLE IMMUNODEFICIENCY; CONSANGUINITY; DIGEORGE SYNDROME; EGYPT; GENETIC ANALYSIS; GRISCELLI SYNDROME; HEALTH SERVICE; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HUMAN; IMMUNE DEFICIENCY; MOLECULAR DIAGNOSIS; MOROCCO; MUCOCUTANEOUS CANDIDIASIS; OCULAR ALBINISM; PATIENT CARE; PHENOTYPE; PREVALENCE; PRIMARY IMMUNODEFICIENCY; REVIEW; SEVERE COMBINED IMMUNODEFICIENCY; SEVERE CONGENITAL NEUTROPENIA; TRANSIENT HYPOGAMMAGLOBULINEMIA OF INFANCY; TUNISIA; WISKOTT ALDRICH SYNDROME;

EID: 82555165268     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2011.06260.x     Document Type: Review

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