Zobrazeno 1 - 10
of 2 198
pro vyhledávání: '"Anhidrosis"'
Autor:
Sanjukta Dasgupta
Publikováno v:
Discover Applied Sciences, Vol 6, Iss 11, Pp 1-13 (2024)
Abstract Eccrine sweat glands are essential for thermoregulation. Acquired idiopathic generalized anhidrosis (AIGA) is a rare disorder characterized by the absence of sweating, leading to severe complications like heatstroke and skin dryness. The und
Externí odkaz:
https://doaj.org/article/2c0906040708439c9d57e7ebfada2bc9
Publikováno v:
Indian Journal of Dermatology. Jul/Aug2020, Vol. 65 Issue 4, p299-303. 5p.
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 10, Pp n/a-n/a (2024)
ABSTRACT Background Congenital insensitivity to pain with anhidrosis (CIPA) (OMIM 256800) is a rare autosomal‐recessive condition, also known as hereditary sensory and autonomic neuropathy type IV (HSAN‐IV). The most commonly reported features in
Externí odkaz:
https://doaj.org/article/992b93d6db4248ab9d5b90aae4efd39b
Autor:
Maria Dolores Robles Urgilez
Publikováno v:
Práctica Familiar Rural, Vol 9, Iss 2 (2024)
La respuesta isotópica de Wolf (WIR) se refiere a la aparición de una nueva enfermedad de la piel en el sitio exacto de una enfermedad de la piel no relacionada que se había curado previamente. Se han descrito varias lesiones cutáneas después de
Externí odkaz:
https://doaj.org/article/8b17175d7276410b9c3efda4e8762568
Autor:
Hanako Miyahara, Noriko Kubota, Mari Okune, Yoshiyuki Ishii, Naoko Okiyama, Toshifumi Nomura, Junichi Furuta
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 7 (2024)
Acquired idiopathic generalized anhidrosis is a rare disease characterized by systemic anhidrosis or hypohidrosis without other systemic diseases. However, its etiology remains unclear. Autoimmune mechanisms seem to be involved in the development of
Externí odkaz:
https://doaj.org/article/f31b4aa44e6c4986aed7420bc7e33cc7
Publikováno v:
Indian Journal of Pain, Vol 38, Iss 1, Pp 69-71 (2024)
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal disorder. It is characterized by systemic insensitivity to pain, unexplained fever, and psychiatric manifestations. Anesthetic management of these cases is a challenge to the
Externí odkaz:
https://doaj.org/article/1733d54191dc4e09baa6d8d8a6c57f7d
Autor:
Herath, Tharuka, Mbydeen, Tsneem H. S., Alagoda, Savindu, Saleh, May, Naidu, Leena, Wimalaratna, Sunil
Publikováno v:
Practical Neurology; Aug2024, Vol. 24 Issue 4, p332-334, 3p
Autor:
Xingzhu Geng1, Yanshan Liu1, XiuZhi Ren2, Yun Guan3, Yanzhou Wang4, Bin Mao1, Xiuli Zhao1 xiulizhao@ibms.pumc.edu.cn, Xue Zhang1 xuezhang@pumc.edu.cn
Publikováno v:
Molecular Pain. 6/8/2018, Vol. 14, p1-11. 11p.
Publikováno v:
The Pan-American Journal of Ophthalmology, Vol 6, Iss 3, Pp 109-109 (2024)
Ross syndrome is a rare clinical entity that manifests classically with a triad of segmental anhidrosis, tonic pupil, and hyporeflexia. Here, we present a case of Ross syndrome in a university-going female in her early twenties with a history of hypo
Externí odkaz:
https://doaj.org/article/11d53259500b4dcc8b5b8db2fd2b1f36
Autor:
Jun Hee Cho, Soojin Hwang, Yoon Hae Kwak, Mi‐Sun Yum, Go Hun Seo, June‐Young Koh, Young Seok Ju, Ji‐Hee Yoon, Minji Kang, Hyo‐Sang Do, Soyoung Kim, Gu‐Hwan Kim, Hyunwoo Bae, Beom Hee Lee
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 4, Pp n/a-n/a (2024)
Abstract Background Congenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder caused by loss‐of‐function mutations of the NTRK1 gene, affecting the autonomic and sensory nervous system. Clinical man
Externí odkaz:
https://doaj.org/article/8da963c2676e4fdb90534c447e635132