Results 91 to 100 of about 7,068 (209)
“Neglected nipples”: acanthosis nigricans-like plaques caused by avoidance of nipple cleansing
Background: Acanthosis nigricans (AN) develops sporadically or in association with obesity, insulin-resistance and dark pigmentary phenotype. Unusual clinical presentations of AN may be diagnostically vexing.
Grazyna Kaminska-Winciore +4 more
doaj +1 more source
Contemporary research pertaining to the prevalence rate of schoolchildren with a skin pigmentation condition called acanthosis nigricans demonstrates that causal factors, such as ethnicity and obesity, can make children more at-risk for obtaining this ...
Walker, Craig A.
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Atypical Presentation of Neuropsychiatric Lupus With Acanthosis Nigricans
Cutaneous manifestations are commonly observed in pediatric patients with systemic lupus erythematosus. Acanthosis nigricans, however, is rarely reported, and even less often in association with neuropsychiatric manifestations of lupus erythematosus.
Lascelles, Karine +4 more
core +1 more source
HUBUNGAN KADAR RESISTIN DENGAN DERAJAT ACANTHOSIS NIGRICANS PADA REMAJA OBESITAS
Latar Belakang. Obesitas pada anak berhubungan dengan meningkatnya risiko penyakit kardiovaskuler dan sindrom metabolik seperti resistensi insulin. Secara klinis, resistensi insulin dapat bermanifestasi sebagai munculan acanthosis nigricans.
DINI, NOVIARTI
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Case Report Hypochondroplasia, Acanthosis Nigricans, and Insulin Resistance in a Child with FGFR3 Mutation: Is It Just an Association? [PDF]
FGFR3 mutations cause wide spectrum of disorders ranging from skeletal dysplasias (hypochondroplasia, achondroplasia, and thanatophoric dysplasia), benign skin tumors (epidermal nevi, seborrhaeic keratosis, and acanthosis nigricans), and epithelial ...
Nabil Moghrabi +2 more
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The acanthosis nigricans form of epidermal nevus
We observed 4 individuals with the acanthosis nigricans (AN) form of epidermal nevus, with clinical and histopathologic features of AN oriented along Blaschko's lines. Three patients had stable lesions since childhood.
Paller, Amy S. +4 more
core +1 more source
[Familial acanthosis nigricans].
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Casado Jimenez, M. +4 more
openaire +2 more sources
Beyond the Obvious: Acanthosis Nigricans as a Clue to the Rare Case of Rabson–Mendenhall Syndrome
Rabson–Mendenhall syndrome (RMS) is a genetic disorder with autosomal recessive inheritance caused by mutations in the insulin receptor (INSR) gene. It is characterized by severe insulin resistance, acanthosis nigricans, skin tags, and growth retardation.
Ashwath Duraiswamy +3 more
doaj +1 more source
Familial acanthosis nigricans due to k650t fgfr3 mutation
Background Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe ...
Berk, David R
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Acanthosis Nigricans: A Clinicoepidemiological and Therapeutic comparison study [PDF]
Acanthosis nigricans is characterized by velvety, brownish black pigmentation of flexural areas. Acanthosis nigricans is considered as a marker of internal diseases like insulin resistance, diabetes, hypothyroidism, polycystic ovarian disease and ...
Balasubramanian, E
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