K. Khadir

Publications110
h-index5
Citations259
Highly Influential Citations12
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Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels.
BACKGROUND Recurrent bacterial and fungal infections, eczema, and increased serum IgE levels characterize patients with the hyper-IgE syndrome (HIES). Known genetic causes for HIES are mutations in… Expand
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Evaluation of the effectiveness of a broad‐spectrum sunscreen in the prevention of chloasma in pregnant women
Background  Chloasma, or melasma, is a pigmentary disorder that can affect between 50% and 70% of pregnant women. During pregnancy, chloasma does not require any particular treatment beside the use… Expand
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Syndrome de Fahr secondaire à une hypoparathyroïdie à révélation dermatologique
Resume Introduction Le syndrome de Fahr est defini par la presence a la base du cerveau de calcifications strio-pallido-dentelees non arteriosclerotiques bilaterales et symetriques. Nous rapportons… Expand
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Macrochéilites granulomateuses : 19 cas
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[Actinomycosic mycetoma of the foot in Morocco due to Actinomycetes viscosus].
We present the case of an actinomycotic mycetoma of the foot due to Actinomycetes viscosus. It evolved for nine years on the foot of a 26-year-old patient from a rural environment: Douar Inezgane… Expand
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[Systemic lupus erythematous: Mortality and prognostic factors in 129 Moroccan patients].
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ERYTHÈME INDURÉ DE BAZIN : 14 OBSERVATIONS AU MAROC, EFFICACITÉ DES ANTI-TUBERCULEUX
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Pyoderma gangrenosum et maladie de Behçet : étude de 2 observations pédiatriques
Resume Le pyoderma gangrenosum (PG) est une dermatose neutrophilique rare qui n’atteint l’enfant que dans 4 % des cas. Elle se caracterise par son association dans la moitie des cas a une maladie… Expand
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[Cutaneous manifestations of male breast cancer].
OBJECTIVE The appearance of skin symptoms in male breast is the main reason for consultation in our context. The aim of this study is to describe the various cutaneous manifestations of male breast… Expand
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Compound heterozygous SLC29A3 mutation causes H syndrome in a Moroccan patient: A case report.
H syndrome is an autosomal recessive syndrome, which affects the skin and some vital organs, it is caused by mutations in the SLC29A3 gene, encoding the human equilibrative nucleoside transporter… Expand
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