The generalized form of acanthosis nigricans, especially in infants, is extremely rare. Herein we report a 1-year-old female child who developed generalized acanthosis nigricans without any evidence of internal malignancy or endocrine disorder. This case is being reported for its rarity
Calcinosis cutis includes dystrophic, metabolic, iatrogenic, and idiopathic subtypes. One variant of...
Acanthosis nigricans (AN) develops sporadically or in association with obesity, insulin-resistance a...
Rabson-Mendenhall syndrome (RMS) is an autosomal recessive disorder due to mutations in the insulin ...
Acanthosis nigricans (OMIM ID % 100600) is a dermatosis characterized by velvety hyperpigmentation, ...
Generalized idiopathic acanthosis nigricans is a rare form of acanthosis nigricans. This form may be...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Acanthosis nigricans (AN) is a skin disorder characterised by skin hyperpigmentation and thickening,...
Nevoid acanthosis nigricans is a rare variant usually presents as a localized hyperpigmented velvety...
Acanthosis nigricans (AN) is a mucocutaneous disorder that is characterized by focal or diffuse hype...
A case is described of a three-day-old female with salt wasting type of 21-hydroxylase deficient con...
Background Acanthosis nigricans is a feature of several syndromes caused by activating mutations of ...
Malignant acanthosis nigricans is associated with extensive lesions and mucosal involvement. It may ...
A girl with a mild sporadic osteochondrodysplasia (OCD) similar to hypochondroplasia but with signif...
International audienceEarly development of extensive acanthosis nigricans (AN) is a key feature in s...
Abstract Background Acanthosis nigricans (AN) is a clinical manifestation featured by velvety brown ...
Calcinosis cutis includes dystrophic, metabolic, iatrogenic, and idiopathic subtypes. One variant of...
Acanthosis nigricans (AN) develops sporadically or in association with obesity, insulin-resistance a...
Rabson-Mendenhall syndrome (RMS) is an autosomal recessive disorder due to mutations in the insulin ...
Acanthosis nigricans (OMIM ID % 100600) is a dermatosis characterized by velvety hyperpigmentation, ...
Generalized idiopathic acanthosis nigricans is a rare form of acanthosis nigricans. This form may be...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Acanthosis nigricans (AN) is a skin disorder characterised by skin hyperpigmentation and thickening,...
Nevoid acanthosis nigricans is a rare variant usually presents as a localized hyperpigmented velvety...
Acanthosis nigricans (AN) is a mucocutaneous disorder that is characterized by focal or diffuse hype...
A case is described of a three-day-old female with salt wasting type of 21-hydroxylase deficient con...
Background Acanthosis nigricans is a feature of several syndromes caused by activating mutations of ...
Malignant acanthosis nigricans is associated with extensive lesions and mucosal involvement. It may ...
A girl with a mild sporadic osteochondrodysplasia (OCD) similar to hypochondroplasia but with signif...
International audienceEarly development of extensive acanthosis nigricans (AN) is a key feature in s...
Abstract Background Acanthosis nigricans (AN) is a clinical manifestation featured by velvety brown ...
Calcinosis cutis includes dystrophic, metabolic, iatrogenic, and idiopathic subtypes. One variant of...
Acanthosis nigricans (AN) develops sporadically or in association with obesity, insulin-resistance a...
Rabson-Mendenhall syndrome (RMS) is an autosomal recessive disorder due to mutations in the insulin ...