Results 1 to 10 of about 4,868 (133)

Chronic Mucocutaneous Candidiasis in Autoimmune Polyendocrine Syndrome Type 1

open access: yesFrontiers in Immunology, 2018
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) is an autosomal recessive disease caused by mutations in the autoimmune regulator (AIRE) gene, characterized by the clinical triad of chronic mucocutaneous candidiasis (CMC ...
Linda Humbert   +10 more
doaj   +3 more sources

Chronic Mucocutaneous Candidiasis: A Case Report

open access: yesClinical, Cosmetic and Investigational Dermatology, 2023
Zhensheng Wang,1 Yongfeng Zhang,1 Weiyuan Ma2 1Department of Pediatrics, Affiliated Hospital of Weifang Medical University, Weifang, People’s Republic of China; 2Department of Dermatology, Affiliated Hospital of Weifang Medical University, Weifang ...
Wang Z, Zhang Y, Ma W
doaj   +2 more sources

Progress in molecular diagnosis and treatment of chronic mucocutaneous candidiasis

open access: yesFrontiers in Immunology
Chronic mucocutaneous candidiasis (CMC) is characterized by recurrent or persistent infections with Candida of the skin, nails, and mucous membrane. It is a rare and severe disease resulting from autoimmune defects or immune dysregulations.
Danrui Jing   +10 more
doaj   +3 more sources

Mucocutaneous and cutaneous generalized candidiasis in a thymectomized dog

open access: yesMedical Mycology Case Reports, 2022
Cutaneous candidiasis is usually related to immunosuppressive diseases and/or therapies as predisposing factors. In humans, chronic mucocutaneous candidiasis (CMC) is observed with thymoma and thymectomy.
Sara Muñoz Declara   +5 more
doaj   +1 more source

Chronic oral mucocutaneous candidiasis, recurrent respiratory infection, hepatosplenomegaly, and autoimmune diabetes mellitus: A case report of a gain-of-function mutation of STAT1 in a Chinese boy

open access: yesFrontiers in Pediatrics, 2022
BackgroundSignal transducer and activator of transcription 1 (STAT1) gain-of-function (GOF) mutations are characterized by chronic mucocutaneous candidiasis and autoimmune diseases.
Bingyan Cao   +3 more
doaj   +1 more source

Chronic mucocutaneous candidiasis: a case with exuberant cutaneous horns in nipples [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2014
Chronic mucocutaneous candidiasis is a rare disorder characterized by persistent and recurrent infections by Candida due to changes in cellular immunity and may be associated with autoimmune endocrine disorders.
Antônio Chambô Filho   +5 more
doaj   +1 more source

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

A novel compound heterozygous mutation of the gene in a patient with autoimmune polyendocrine syndrome type 1 [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism, 2019
Autoimmune polyendocrine syndrome type 1 (APS-1), or autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy is a rare, autosomal recessive autoimmune disease caused by a mutation of the autoimmune regulator (AIRE) gene.
Junghwan Suh   +5 more
doaj   +1 more source

Gain-of-function STAT1 mutation and visceral leishmaniasis

open access: yesEinstein (São Paulo), 2022
Gain-of-function mutations in the STAT1 gene have been initially associated with chronic mucocutaneous candidiasis. However, further research has shown that STAT1 GOF variants may increase susceptibility to infection by other intracellular pathogens ...
Paula Teixeira Lyra   +6 more
doaj   +1 more source

Chronic Mucocutaneous Candidiasis as Primary Immunodeficiency in Children

open access: yesZdorovʹe Rebenka, 2013
Chronic mucocutaneous candidiasis is a genetically heterogeneous group of disorders associated with mutations in genes STAT1, IL17RA, IL17F, AIRE, STAT3, TYK2, IL12RB1, and IL12B.
L.I. Chernyshova   +5 more
doaj   +1 more source

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