2011
DOI: 10.1016/j.arcped.2011.06.015
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La cryptosporidiose chez les enfants atteints de déficits immunitaires primitifs par défaut d’expression de protéines du complexe majeur d’histocompatibilité classe II en Tunisie : à propos de 5 observations

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Cited by 8 publications
(3 citation statements)
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References 23 publications
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“…Some C. parvum subtypes have been reported to be human-adapted subtypes, that could be transmitted from person to person, with origins from humans (Morse et al 2007). The reporting of C. meleagridis in this study is not surprising, as the African population has a growing immune-compromised population with a previous report of 21% in these populations prone to infection by this pathogen (Morgan et al 2000;Ben Abda et al 2011;Aldeyarbi et al 2016). Cryptosporidial infection was observed to be highest among HIV/AIDS patients, followed by children and then diarrhoeic individuals.…”
Section: Discussionsupporting
confidence: 61%
“…Some C. parvum subtypes have been reported to be human-adapted subtypes, that could be transmitted from person to person, with origins from humans (Morse et al 2007). The reporting of C. meleagridis in this study is not surprising, as the African population has a growing immune-compromised population with a previous report of 21% in these populations prone to infection by this pathogen (Morgan et al 2000;Ben Abda et al 2011;Aldeyarbi et al 2016). Cryptosporidial infection was observed to be highest among HIV/AIDS patients, followed by children and then diarrhoeic individuals.…”
Section: Discussionsupporting
confidence: 61%
“…In immunocompromised individuals, the prevalence of C. meleagridis can reach 75% (3/4 of samples typed) [23, 25, 101, 146, 147, 151, 152], but also 75% (9/12 of samples typed) in immunocompetent individuals [86, 106, 114, 141, 149, 153, 155, 156]. In comparison, the prevalence of C. meleagridis in the developed world is ~1% [66].…”
Section: Cryptosporidium and Giardia Species Reported In Humans In Afmentioning
confidence: 99%
“…Founder effect for the c.338-25_338del26 mutation in the RFXANK gene in 25 patients Landouré et al [47] (2013) Mali 3 patients from 1 Malian family Ataxia-telangiectasia Novel c.7985T > A mutation in ATM gene Djidjik et al [48] (2012) Algeria 11 Algerian patients MHC class II expression deficiency Founder effect for the 752delG26 mutation in RFXANK gene in 9 patients Naamane et al [49] (2010) Morocco 10 Moroccan patients MHC class II expression deficiency Founder effect for the 752delG26 mutation in the RFXANK gene in 10 patients El Kares et al [50] (2006) Tunisia 15 Tunisian patients CGD Two novel and recurrent mutations in NCF2 and CYBA gene Pienaar et al [51] (2003) SA 2 SA patients Hyper IgM First report of X-linked hyper IgM (HIGM1) from SA Elloumi-Zghal et al [52] (2002) Tunisia 5 Tunisian patients MSMD IL-12Rb1 gene mutation in 2 patients and IL-12p40 gene mutation in 3 patients; first description of familial cytokine deficiency Eley BS et al [53] (2001) SA 5 SA patients SCID 3 with IL-2RγC deficiency; 1 with RAG1 deficiency 1 with IL-7Rα deficiency Pienaar et al [54] There are additional scattered studies from the region describing PID, including patients' susceptibilities to various infections and case reports. [61][62][63][64][65][66][67][68]…”
Section: Mhc Class II Expression Deficiencymentioning
confidence: 99%