Results 1 to 10 of about 5,874 (223)

Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report [PDF]

Clinics and Practice
Background: Adverse reactions to tattoo pigments are increasingly recognized, yet severe systemic complications remain rare and poorly characterized. Red tattoo ink, in particular, is associated with delayed hypersensitivity reactions, but widespread ...
Mateusz K. Mateuszczyk, Magdalena Łyko, Andrzej Bieniek, Joanna Maj, Alina Jankowska-Konsur   +4 more
doaj   +2 more sources

Acquired idiopathic generalized anhidrosis

Indian 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, Sebastian Criton, Divya Surendran   +2 more
doaj   +3 more sources

Congenital Insensitivity to Pain With Anhidrosis: First Reported Case in Nepal [PDF]

Clinical Case Reports
Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder characterized by anhidrosis, self‐mutilation, and insensitivity to pain and temperature.
Sobin Pant, Dibij Adhikari, Prakash Pandey, Binit Bajracharya, Rizuna Sharma   +4 more
doaj   +2 more sources

Ross syndrome following COVID-19 infection in an 18-year-old Syrian male patient: a case report [PDF]

Journal of Medical Case Reports
Background Ross syndrome is an exceptionally rare disorder characterized by tonic pupils, areflexia, and anhidrosis, with a prevalence that appears to be higher in women than in men, typically presenting in individuals during their 30s.
Ahed Assaf, Suleiman Khaddour, William Borghol, Saja Karaja, Faisal Alfaksh, Khayry Al-Shami   +5 more
doaj   +2 more sources

Orthostatic Hypotension, Anhidrosis, and Impotence [PDF]

Circulation, 1952
Anhidrosis and impotence occur frequently with idiopathic orthostatic hypotension. Two new cases of this syndrome, which occurs chiefly in males over 40 years of age, are herewith described. Postural vertigo and/or syncope, weakness, and anhidrosis or hypohidrosis are common symptoms, and a marked fall in systolic and diastolic blood pressure is noted ...
M, ROSECAN, R J, GLASER, M L, GOLDMAN
exaly   +3 more sources

Ion Channel and Ubiquitin Differential Expression during Erythromycin-Induced Anhidrosis in Foals

Animals, 2021
Macrolide drugs are the treatment of choice for Rhodococcus equi infections, despite severe side-effects temporary anhidrosis as a. To better understand the molecular biology leading to macrolide induced anhidrosis, we performed skin biopsies and ...
Laura Patterson Rosa, Martha F. Mallicote, Robert J. MacKay, Samantha A. Brooks   +3 more
doaj   +1 more source

Case Report: Acquired Generalized Anhidrosis Caused by Brain Tumor: Review of the Literature

Frontiers in Endocrinology, 2022
PurposeThere has been limited focus on sweating failure in patients with brain tumor. We report two patients with generalized anhidrosis caused by germinoma. We also review previous reports of generalized anhidrosis due to brain tumor.Case ReportsPatient
Kohei Kawahara, Yasuto Shimomura, Yuichiro Oshima, Tadashi Watanabe, Toshinori Hori, Akihisa Okumura, Hideyuki Iwayama   +6 more
doaj   +1 more source

Manifestaciones clínicas de la insensibilidad congénita al dolor con anhidrosis

Salud Uninorte, 2020
Introducción: La insensibilidad congénita al dolor con anhidrosis (HSAN IV o CIPA) es una enfermedad rara con sintomatologia multisistémica, que impacta el funcionamiento cognitivo, y afecta negativamente la calidad de vida los pacientes y sus familias.
YANIN ELENA SANTOYA MONTES, PEDRO PUENTES ROZO   +1 more
doaj   +1 more source

Sisters with no pain, no tears: A report of a new variant of hereditary sensory and autonomic neuropathy (Type IX) Caused by a novel SCN11A mutation

Indian Journal of Dermatology, 2020
Lack of pain sensation in children involves a rare group of heritable disorders; hereditary sensory and autonomic neuropathy (HSAN). Till date, eight types of HSAN have been described depending on the clinical phenotype and the underlying gene mutation ...
Shital Poojary, Saurabh Jaiswal, Kapisha Sunny Shah, Krishna B Bhalala   +3 more
doaj   +1 more source

Ross syndrome and diabetes mellitus: An interesting association

Clinical Dermatology Review, 2020
Ross syndrome is a rare disorder of sweating with a triad of segmental anhidrosis, tonic pupil, and hyporeflexia. Survey of available literature shows scarce reporting of such cases globally and countable number of cases from India.
Chetan D Rajput, Sanjay B Gore, Shailesh S Malani, Swagat M Shah   +3 more
doaj   +1 more source