Congenital Insensitivity to Pain With Anhidrosis: First Reported Case in Nepal [PDF]
Clinical Case Reports (discontinued)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 +4 more
exaly +3 more sources
Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report [PDF]
Clinics and PracticeBackground: 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 +4 more
doaj +2 more sources
CCL22-producing macrophages are associated with Th1-related sweat duct inflammation in acquired idiopathic generalized anhidrosis [PDF]
Frontiers in ImmunologyBackgroundAcquired 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
Early clinical diagnosis of congenital insensitivity to pain with anhidrosis in an infant: a case report [PDF]
Frontiers in PediatricsCongenital insensitivity to pain with anhidrosis (CIPA) is an extremely rare autosomal recessive disorder. Its core clinical manifestations include profound pain insensitivity, generalized anhidrosis, and subsequent recurrent hyperthermia.
Ziqing Tang +7 more
doaj +2 more sources
X‐Linked Anhidrotic Ectodermal Dysplasia in A 19‐Year‐Old Male: A Classic Phenotype [PDF]
Clinical Case ReportsX‐linked anhidrotic/hypohidrotic ectodermal dysplasia (XLHED), also known as Christ‐Siemens‐Touraine syndrome, is a rare genetic disorder characterized by the abnormal development of ectodermal structures, primarily affecting sweat glands, hair, and ...
Laxman Chapagain +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 ReportsBackground 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 +5 more
doaj +2 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 +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 +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 +1 more
doaj +1 more source
Congenital insensitivity to pain with anhidrosis and compensatory hyperhidrosis
Indian Journal of Paediatric Dermatology, 2021 Hereditary sensory and autonomic neuropathy is a rare syndrome characterized by congenital insensitivity to pain, temperature changes, and an autonomic nerve formation disorder. We report an 8-year-old boy who presented with late-onset of self-mutilating
Aradhana Rout +3 more
doaj +1 more source