نتایج جستجو برای: erythromelalgia

تعداد نتایج: 422  

Journal: :Molecular Pain 2008
Xiaoyang Cheng Sulayman D Dib-Hajj Lynda Tyrrell Stephen G Waxman

BACKGROUND Primary erythromelalgia is an autosomal dominant pain disorder characterized by burning pain and skin redness in the extremities, with onset of symptoms during the first decade in the families whose mutations have been physiologically studied to date. Several mutations of voltage-gated Na+ channel NaV1.7 have been linked with primary erythromelalgia. Recently, a new substitution Na(v...

Journal: :Archives of dermatology 2006
Mark D P Davis Joseph Genebriera Paola Sandroni Robert D Fealey

OBJECTIVES To examine the results of thermoregulatory sweat testing in patients with erythromelalgia and to compare them with the results of other neurophysiologic tests of small-fiber nerve function. DESIGN Retrospective study. SETTING Tertiary referral center. PATIENTS Thirty-two consecutive patients with erythromelalgia who had thermoregulatory sweat testing in addition to vascular and...

Journal: :Brain : a journal of neurology 2009
Chongyang Han Sulayman D Dib-Hajj Zhimiao Lin Yan Li Emmanuella M Eastman Lynda Tyrrell Xianwei Cao Yong Yang Stephen G Waxman

Inherited erythromelalgia (IEM), an autosomal dominant disorder characterized by severe burning pain in response to mild warmth, has been shown to be caused by gain-of-function mutations of sodium channel Na(v)1.7 which is preferentially expressed within dorsal root ganglion (DRG) and sympathetic ganglion neurons. Almost all physiologically characterized cases of IEM have been associated with o...

Journal: :Molecular Pain 2007
Chongyang Han Angelika Lampert Anthony M Rush Sulayman D Dib-Hajj Xiaoliang Wang Yong Yang Stephen G Waxman

BACKGROUND The disabling chronic pain syndrome erythromelalgia (also termed erythermalgia) is characterized by attacks of burning pain in the extremities induced by warmth. Pharmacological treatment is often ineffective, but the pain can be alleviated by cooling of the limbs. Inherited erythromelalgia has recently been linked to mutations in the gene SCN9A, which encodes the voltage-gated sodiu...

2018
María Bibiana Leroux

The low prevalence of erythromelalgia, classified as an orphan disease, poses diagnostic and therapeutic difficulties. The aim of this review is to be an update of the specialized bibliography. Erythromelalgia is an infrequent episodic acrosyndrome affecting mainly both lower limbs symmetrically with the classic triad of erythema, warmth and burning pain. Primary erythromelalgia is an autosomal...

Journal: :Proceedings of the Royal Society of Medicine 1909

2015
Jan J. Michiels

Primary or idiopathic erythermalgia is characterized by recurrent, red, warm, and painful lower extremities. It arises at young age and persists throughout life because no treatment is available. We report the cutaneous pathology of affected skin lesions of three patients with primary erythermalgia. Biopsy specimens showed a mild perivascular mononuclear infiltrate, thickened blood vessel basem...

Journal: :Archives of Dermatology 2000

Journal: :Actas Dermo-Sifiliográficas (English Edition) 2020

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