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Page 1
Drug-induced hyperhidrosis and hypohidrosis: incidence, prevention and management.
Cheshire WP, Fealey RD. Cheshire WP, et al. Drug Saf. 2008;31(2):109-26. doi: 10.2165/00002018-200831020-00002. Drug Saf. 2008. PMID: 18217788 Review.
The symptom of dry mouth often accompanies the less apparent symptom of hypohidrosis because the muscarinic M(3) acetylcholine receptor type predominates at both sweat and salivary glands. ...Advances in the understanding of drug-induced anhidrosis have also enlarged the …
The symptom of dry mouth often accompanies the less apparent symptom of hypohidrosis because the muscarinic M(3) acetylcholine recept …
Fabry's disease--a comprehensive review on pathogenesis, diagnosis and treatment.
Mahmud HM. Mahmud HM. J Pak Med Assoc. 2014 Feb;64(2):189-94. J Pak Med Assoc. 2014. PMID: 24640811 Review.
Fabry's deposits are defined histopathologically as lamellate membrane like structure called myeloid or Zebra bodies. Clinical manifestations of disease are hypohidrosis, acroparesthesias, heat intolerance, angiokeratomas, corneal opacities, cardiac arrhythmias, left ventr …
Fabry's deposits are defined histopathologically as lamellate membrane like structure called myeloid or Zebra bodies. Clinical manifestation …
Treatment of Anderson-Fabry Disease.
Simonetta I, Tuttolomondo A, Daidone M, Miceli S, Pinto A. Simonetta I, et al. Curr Pharm Des. 2020;26(40):5089-5099. doi: 10.2174/1381612826666200317142412. Curr Pharm Des. 2020. PMID: 32183665 Review.
The current treatment of Anderson-Fabry disease is represented by enzyme replacement therapy (ERT) and oral pharmacological chaperone. Future treatments are based on new strategic approaches such as stem cell-based therapy, pharmacological approaches chaperones, mRN …
The current treatment of Anderson-Fabry disease is represented by enzyme replacement therapy (ERT) and oral pharmacological chaperone …
Isolated hypohidrosis: pathogenesis and treatment.
Chan MMH, Lim GH, Zhao X, Tey HL. Chan MMH, et al. Eur J Dermatol. 2020 Dec 1;30(6):680-687. doi: 10.1684/ejd.2020.3931. Eur J Dermatol. 2020. PMID: 33262099
The majority of hypohidrosis cases have no associated abnormalities or secondary causes, and are termed "isolated hypohidrosis". ...OBJECTIVES: To elucidate the pathogenesis of isolated hypohidrosis using in vivo high-definition optical coherence tomography ( …
The majority of hypohidrosis cases have no associated abnormalities or secondary causes, and are termed "isolated hypohidrosis …
Fabry disease: Review and experience during newborn screening.
Hsu TR, Niu DM. Hsu TR, et al. Trends Cardiovasc Med. 2018 May;28(4):274-281. doi: 10.1016/j.tcm.2017.10.001. Epub 2017 Oct 20. Trends Cardiovasc Med. 2018. PMID: 29100912 Review.
Affected males with classic FD have little or no enzyme activity and have an early onset of symptoms and signs, including acroparesthesias, hypohidrosis, angiokeratomas, gastrointestinal dysfunction and/or a characteristic corneal dystrophy during childhood/adolescence. .. …
Affected males with classic FD have little or no enzyme activity and have an early onset of symptoms and signs, including acroparesthesias, …
The management and treatment of children with Fabry disease: A United States-based perspective.
Hopkin RJ, Jefferies JL, Laney DA, Lawson VH, Mauer M, Taylor MR, Wilcox WR; Fabry Pediatric Expert Panel. Hopkin RJ, et al. Mol Genet Metab. 2016 Feb;117(2):104-13. doi: 10.1016/j.ymgme.2015.10.007. Epub 2015 Oct 23. Mol Genet Metab. 2016. PMID: 26546059 Review.
Fabry disease is an inherited X-linked disorder that presents during childhood in male and female patients. Young patients may initially experience pain, hypohidrosis, and gastrointestinal symptoms. Other manifestations of Fabry disease, such as renal and cardiac disease, …
Fabry disease is an inherited X-linked disorder that presents during childhood in male and female patients. Young patients may initially exp …
Clinical Analysis and Management of Acquired Idiopathic Generalized Anhidrosis.
Satoh T. Satoh T. Curr Probl Dermatol. 2016;51:75-9. doi: 10.1159/000446781. Epub 2016 Aug 30. Curr Probl Dermatol. 2016. PMID: 27584965 Review.
Acquired idiopathic generalized anhidrosis (AIGA) is a sweating disorder characterized by inadequate sweating in response to heat stimuli such as high temperature, humidity, and physical exercise. Patients exhibit widespread nonsegmental hypohidrosis/anhidrosis without any …
Acquired idiopathic generalized anhidrosis (AIGA) is a sweating disorder characterized by inadequate sweating in response to heat stimuli su …
Hypohidrotic Ectodermal Dysplasia Milia Treatment With Fractional Carbon Dioxide Laser and Laser-Assisted Drug Delivery of Triamcinolone.
Mineroff J, Dowling JR, Golbari NM, Wechter T, Jagdeo J. Mineroff J, et al. J Drugs Dermatol. 2023 Nov 1;22(11):1130-1132. doi: 10.36849/JDD.7650. J Drugs Dermatol. 2023. PMID: 37943264
Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder characterized by hypohidrosis, hypodontia, and hypotrichosis. Skin manifestations, including dyspigmentation and milia-like papules that coalesce into plaques, are difficult to treat. ...The facial skin rashes c …
Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder characterized by hypohidrosis, hypodontia, and hypotrichosis. Skin mani …
Cholinergic urticaria: epidemiology, physiopathology, new categorization, and management.
Fukunaga A, Washio K, Hatakeyama M, Oda Y, Ogura K, Horikawa T, Nishigori C. Fukunaga A, et al. Clin Auton Res. 2018 Feb;28(1):103-113. doi: 10.1007/s10286-017-0418-6. Epub 2017 Apr 5. Clin Auton Res. 2018. PMID: 28382552 Review.
METHODS: Using an integrative approach, we reviewed publications addressing the epidemiology, clinical features, diagnostic approach, physiopathology, subtype classification, and therapeutic approach to cholinergic urticaria. RESULTS: Multiple mechanisms were found to cont …
METHODS: Using an integrative approach, we reviewed publications addressing the epidemiology, clinical features, diagnostic approach, physio …
Cholinergic urticaria: pathogenesis-based categorization and its treatment options.
Nakamizo S, Egawa G, Miyachi Y, Kabashima K. Nakamizo S, et al. J Eur Acad Dermatol Venereol. 2012 Jan;26(1):114-6. doi: 10.1111/j.1468-3083.2011.04017.x. Epub 2011 Mar 4. J Eur Acad Dermatol Venereol. 2012. PMID: 21371134 Review.
CONCLUSIONS: In this review, we categorize CU into four subtypes: (i) CU with poral occlusion; (ii) CU with acquired generalized hypohidrosis; (iii) CU with sweat allergy; and (iv) idiopathic CU, and discuss diagnostic and treatment options....
CONCLUSIONS: In this review, we categorize CU into four subtypes: (i) CU with poral occlusion; (ii) CU with acquired generalized hypohidr …
25 results