Human protothecosis is a rare microalgae infection, and its dissemination typically occurs in immunocompromised individuals, but no specific immune defect has been reported. Here, we describe an 8-year-old daughter of a consanguineous union with abdominal pain and bloody diarrhea for 3 months who was found to have pancolitis with numerous microalgae identified as Prototheca zopfii. In the absence of a known immunodeficiency, exome sequencing was performed, which uncovered a novel recessive frameshift mutation in CARD9 (p.V261fs). This report highlights that CARD9 deficiency should be investigated in patients with unexplained systemic/visceral protothecosis and suggests a new mechanistic insight into anti-Prototheca immunity
Chronic mucocutaneous candidiasis is a primary immunodeficiency characterized by persistent or recur...
CARD9 is a signaling adaptor protein that is involved in the transduction of signals from a variety ...
We described for the first time a female patient with the simultaneous presence of two homozygous mu...
Human protothecosis is a rare microalgae infection, and its dissemination typically occurs in immuno...
Exophiala species are mostly responsible for skin infections. Invasive Exophiala dermatitidis diseas...
International audienceBackground. Exophiala species are mostly responsible for skin infections. Inva...
Abstract: Autosomal recessive CARD9 deficiency underlies life-threatening, invasive fungal infection...
Background. Exophiala species are mostly responsible for skin infections. Invasive Exophiala dermati...
CARD9 mutations are known to predispose patients to phaeohyphomycosis caused by different dematiaceo...
BACKGROUND: Invasive infections of the central nervous system (CNS) or digestive tract caused by com...
Invasive infections of the central nervous system or digestive tract caused by commensal fungi of th...
Chronic mucocutaneous or invasive fungal infections are generally the result of primary or secondary...
International audienceBACKGROUND:Invasive infections of the central nervous system (CNS) or digestiv...
Autosomal recessive (AR) CARD9 (caspase recruitment domain-containing protein 9) deficiency underlie...
Autosomal recessive deficiency in the caspase recruitment domain containing protein 9 (CARD9) result...
Chronic mucocutaneous candidiasis is a primary immunodeficiency characterized by persistent or recur...
CARD9 is a signaling adaptor protein that is involved in the transduction of signals from a variety ...
We described for the first time a female patient with the simultaneous presence of two homozygous mu...
Human protothecosis is a rare microalgae infection, and its dissemination typically occurs in immuno...
Exophiala species are mostly responsible for skin infections. Invasive Exophiala dermatitidis diseas...
International audienceBackground. Exophiala species are mostly responsible for skin infections. Inva...
Abstract: Autosomal recessive CARD9 deficiency underlies life-threatening, invasive fungal infection...
Background. Exophiala species are mostly responsible for skin infections. Invasive Exophiala dermati...
CARD9 mutations are known to predispose patients to phaeohyphomycosis caused by different dematiaceo...
BACKGROUND: Invasive infections of the central nervous system (CNS) or digestive tract caused by com...
Invasive infections of the central nervous system or digestive tract caused by commensal fungi of th...
Chronic mucocutaneous or invasive fungal infections are generally the result of primary or secondary...
International audienceBACKGROUND:Invasive infections of the central nervous system (CNS) or digestiv...
Autosomal recessive (AR) CARD9 (caspase recruitment domain-containing protein 9) deficiency underlie...
Autosomal recessive deficiency in the caspase recruitment domain containing protein 9 (CARD9) result...
Chronic mucocutaneous candidiasis is a primary immunodeficiency characterized by persistent or recur...
CARD9 is a signaling adaptor protein that is involved in the transduction of signals from a variety ...
We described for the first time a female patient with the simultaneous presence of two homozygous mu...