Results 1 to 10 of about 265 (106)

Acquired idiopathic generalized anhidrosis [PDF]

open access: yesIndian Journal of Dermatology, 2015
Acquired idiopathic generalized anhidrosis is a rare condition, where the exact pathomechanism is unknown. We report a case of acquired idiopathic generalized anhidrosis in a patient who later developed lichen planus.
Geethu Gangadharan   +2 more
doaj   +4 more sources

Acquired idiopathic generalized anhidrosis in a young Austrian patient [PDF]

open access: yesJAAD Case Reports, 2018
Acquired idiopathic generalized anhidrosis (AIGA) is a rare disease with approximately 100 reported cases worldwide, many of which occurred in Asia, especially in Japan.1 To diagnose AIGA, other causes of anhidrosis (medications; physical agents; and dermatologic, neurologic, metabolic, and endocrine disorders), must be ruled out.
Christa Pargfrieder, MD   +5 more
doaj   +5 more sources

Acquired Idiopathic Generalized Anhidrosis (AIGA) and Its Complications: Implications for AIGA as an Autoimmune Disease [PDF]

open access: yesInternational Journal of Molecular Sciences, 2021
Acquired idiopathic generalized anhidrosis (AIGA) is a rare disorder in which systemic anhidrosis/hypohidrosis occurs without causative dermatological, metabolic or neurological disorder. Most cases of AIGA have been reported in Asia, especially in Japan, but there have been only a few reports in Europe and the United States.
Tetsuya Honda
exaly   +5 more sources

A Case of Acquired Idiopathic Generalized Anhidrosis with Anti-mucin 7 Seropositivity [PDF]

open access: yesActa Dermato-Venereologica
Marie Kitamura   +4 more
doaj   +4 more sources

Photoletter to the editor: Acquired idiopathic generalized anhidrosis. [PDF]

open access: yesJ Dermatol Case Rep, 2014
Anhidrosis is a failure in sweat production in response to physiological thermal or chemical stimuli. Acquired idiopathic generalized anhidrosis is a rare disorder without sweat gland pathology and without neurologic symptoms. Most cases have been reported from Far East.
Wollina U.
europepmc   +4 more sources

CCL22-producing macrophages are associated with Th1-related sweat duct inflammation in acquired idiopathic generalized anhidrosis [PDF]

open access: yesFrontiers in Immunology
BackgroundAcquired idiopathic generalized anhidrosis (AIGA) is a rare disorder characterized by generalized loss of sweating without identifiable causes.
Shingo Takei   +5 more
doaj   +2 more sources

Prognosis after steroid pulse therapy and seasonal effect in acquired idiopathic generalized anhidrosis. [PDF]

open access: yesJ Dermatol, 2021
Abstract Acquired idiopathic generalized anhidrosis is a rare disease with unknown etiology. Sudden loss of sweating function adversely affects young patients’ quality of life. Although systemic corticosteroid therapy is the most frequently reported treatment for the disease, its effectiveness is controversial because of the risk of ...
Iida T   +10 more
europepmc   +4 more sources

Idiopathic Acquired Anhidrosis: Reversible Generalized Anhidrosis after Sunstroke

open access: yesJournal of Dermatology, 1999
AbstractIdiopathic acquired generalized anhidrosis is a very rare condition in which the pathogenesis is still unknown. Although varied findings have been reported, no consistent abnormal findings in sweat glands have been established by histological study or electronmicroscopic study.
Seung Hun Lee
exaly   +4 more sources

Involvement of TRPV4 in temperature-dependent perspiration in mice [PDF]

open access: yeseLife
Reports indicate that an interaction between TRPV4 and anoctamin 1 (ANO1) could be widely involved in water efflux of exocrine glands, suggesting that the interaction could play a role in perspiration.
Makiko Kashio   +6 more
doaj   +2 more sources

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