Chronic and Invasive Fungal Infections in a Family with CARD9 Deficiency

Journal of Clinical Immunology

Volumn 36, Issue 3, 2016, Pages 204-209

  Alves de Medeiros, Ana Karina ^a   Lodewick, Evelyn ^a   Bogaert, Delfien J A ^a   Haerynck, Filomeen ^a   Van daele, Sabine ^a   Lambrecht, Bart ^a,b   Bosma, Sara ^a   Vanderdonckt, Laure ^a   Lortholary, Olivier ^c,d   Migaud, Mélanie ^c,e   Casanova, Jean Laurent ^c,d,e,f,g   Puel, Anne ^c,e   Lanternier, Fanny ^c,d,e   Lambert, Jo ^a   Brochez, Lieve ^a   Dullaers, Melissa ^a,b  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c UNIVERSITÉ PARIS DESCARTES   (France)

^d HÔPITAL NECKER ENFANTS MALADES   (France)

^e IMAGINE INSTITUTE   (France)

^f ROCKEFELLER UNIVERSITY   (United States)

^g HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

Autosomal recessive CARD9 deficiency; Chronic mucocutaneous candidiasis; Cutaneous and deep dermatophytosis

Indexed keywords

AMPHOTERICIN B; CARRIER PROTEINS AND BINDING PROTEINS; CASPASE RECRUITMENT DOMAIN CONTAINING PROTEIN 9; FLUCONAZOLE; FLUCYTOSINE; GLUCOSE; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; GRISEOFULVIN; IMMUNOGLOBULIN E; INTERLEUKIN 17; INTERLEUKIN 22; INTERLEUKIN 6; ITRACONAZOLE; KETOCONAZOLE; STAT1 PROTEIN; STAT3 PROTEIN; TERBINAFINE; UNCLASSIFIED DRUG; CARD9 PROTEIN, HUMAN; CASPASE RECRUITMENT DOMAIN SIGNALING PROTEIN; IL6 PROTEIN, HUMAN; INTERLEUKIN DERIVATIVE; INTERLEUKIN-22;

ADULT; ARTICLE; AXILLARY LYMPH NODE; BRAIN INFARCTION; CANDIDA ALBICANS; CANDIDIASIS; CASE REPORT; CD4+ T LYMPHOCYTE; CEREBROSPINAL FLUID ANALYSIS; COMPUTER ASSISTED TOMOGRAPHY; CONSANGUINEOUS MARRIAGE; CYTOKINE PRODUCTION; CYTOKINE RELEASE; DERMATOPHYTOSIS; ENCEPHALITIS; ENDOCRINE DISEASE; EOSINOPHILIA; GENE MUTATION; GENETIC SCREENING; GLUCOSE BLOOD LEVEL; HEMIPLEGIA; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HYPER IGE SYNDROME; IMMUNOHISTOCHEMISTRY; INTERNAL CAROTID ARTERY ANEURYSM; LEUKOCYTE COUNT; LYMPHADENOPATHY; MALASSEZIA FURFUR; MALE; MIDDLE AGED; MISSENSE MUTATION; MONONUCLEAR CELL; MUCOCUTANEOUS CANDIDIASIS; NONHUMAN; ONYCHOMYCOSIS; PERIPHERAL BLOOD MONONUCLEAR CELL; PHENOTYPE; POLYMORPHONUCLEAR CELL; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; RECURRENT INFECTION; SKIN CULTURE; SKIN DEFECT; SYSTEMIC MYCOSIS; THRUSH; TINEA CAPITIS; TINEA CORPORIS; TINEA VERSICOLOR; TRICHOPHYTON RUBRUM; TRICHOPHYTON RUBRUM INFECTION; TRICHOPHYTON VERRUCOSUM; TRICHOPHYTON VERRUCOSUM INFECTION; TRICHOPHYTON VIOLACEUM; TRICHOPHYTON VIOLACEUM INFECTION; TURKISH CITIZEN; CANDIDA; CHILD; CONSANGUINITY; DEFICIENCY; FEMALE; GENE EXPRESSION; GENETIC PREDISPOSITION; GENETICS; GROWTH, DEVELOPMENT AND AGING; HOMOZYGOTE; IMMUNE DEFICIENCY; IMMUNOLOGY; MUTATION; PATHOGENICITY; PATHOLOGY; PEDIGREE; RECESSIVE GENE; T LYMPHOCYTE; TINEA; TRICHOPHYTON; TURKEY;

CANDIDA; CANDIDIASIS, CHRONIC MUCOCUTANEOUS; CARD SIGNALING ADAPTOR PROTEINS; CHILD; CONSANGUINITY; FEMALE; GENE EXPRESSION; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; HOMOZYGOTE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INTERLEUKIN-17; INTERLEUKIN-6; INTERLEUKINS; INVASIVE FUNGAL INFECTIONS; MALE; MIDDLE AGED; MUTATION; PEDIGREE; T-LYMPHOCYTES; TINEA; TRICHOPHYTON; TURKEY;

EID: 84961140374     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-016-0255-8     Document Type: Article

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