Anhidrosis: Difference between revisions
m Bot: Removing from Primary care |
|||
(7 intermediate revisions by 5 users not shown) | |||
Line 1: | Line 1: | ||
__NOTOC__ | |||
{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}} | ||
{{SK}} Hypohidrosis; oligidria; oligohidrosis; sweating deficiency | |||
==Overview== | |||
'''Anhidrosis''' means lack of [[sweating]]. | |||
==Causes== | |||
It may be caused by underactivity of the [[sympathetic nervous system]]. Eccrine sweat glands are [[nerve|innervated]] by [[muscarinic acetylcholine receptor]]s. Therefore, antimuscarinic [[medication|drugs]] can cause anhidrosis. | |||
===Common Causes=== | |||
* Miscellaneous conditions | |||
** [[Ross syndrome]] | |||
* Symptoms and signs | |||
** [[Horner syndrome]] | |||
** [[Chromosomal abnormalities]] | |||
** [[Chromosome 22q13.3 deletion syndrome]] | |||
* Autosomal dominant conditions | |||
** [[Dermatopathia pigmentosa reticularis]] | |||
** [[Hay-Wells syndrome]] | |||
** Hereditary sensory and autonomic neuropathy type 1E | |||
** Hypohidrotic ectodermal dysplasia, autosomal dominant | |||
** Limb-mammary syndrome | |||
** Marshall syndrome | |||
** Naegeli-Franceschetti-Jadassohn syndrome | |||
** Rapp-Hodgkin ectodermal dysplasia syndrome | |||
* Autosomal recessive conditions | |||
** Hereditary sensory and autonomic neuropathy type 4 | |||
** Hypohidrotic ectodermal dysplasia, autosomal recessive type | |||
** [[Rosselli-Gulienetti syndrome]] | |||
* X-linked inherited conditions | |||
** Bazex-Dupre-Christol syndrome | |||
** Hypohidrotic ectodermal dysplasia with immune deficiency | |||
** Hypohidrotic ectodermal dysplasia, X-linked | |||
* Bacteria and bacterial conditions | |||
** [[Lepromatous leprosy]] | |||
** [[Tuberculoid leprosy]] | |||
* Iatrogenic conditions | |||
** [[Sympathectomy]] | |||
** [[Drug]]s, [[hormone]]s and mediators | |||
** [[Hexamethonium]] | |||
** [[Topiramate]] | |||
** [[Zonisamide]] | |||
* Drug Causes | |||
** [[Benztropine Mesylate]] | |||
** [[Propantheline bromide]] | |||
== | ==Related Chapters== | ||
* [[Horner's syndrome]] | * [[Horner's syndrome]] | ||
* [[Hyperhidrosis|Hyperhidrosis (excessive sweating)]] | * [[Hyperhidrosis|Hyperhidrosis (excessive sweating)]] | ||
Line 29: | Line 59: | ||
==References== | ==References== | ||
{{Reflist}} | {{Reflist}} | ||
{{Diseases of the skin and subcutaneous tissue}} | |||
[[de:Anhidrose]] | [[de:Anhidrose]] | ||
[[pl:Anhydroza]] | [[pl:Anhydroza]] | ||
Line 45: | Line 67: | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Medical terms]] | |||
[[Category:Dermatology]] |
Latest revision as of 20:24, 29 July 2020
WikiDoc Resources for Anhidrosis |
Articles |
---|
Most recent articles on Anhidrosis |
Media |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Anhidrosis at Clinical Trials.gov Clinical Trials on Anhidrosis at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Anhidrosis
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Anhidrosis Discussion groups on Anhidrosis Patient Handouts on Anhidrosis Directions to Hospitals Treating Anhidrosis Risk calculators and risk factors for Anhidrosis
|
Healthcare Provider Resources |
Causes & Risk Factors for Anhidrosis |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Hypohidrosis; oligidria; oligohidrosis; sweating deficiency
Overview
Anhidrosis means lack of sweating.
Causes
It may be caused by underactivity of the sympathetic nervous system. Eccrine sweat glands are innervated by muscarinic acetylcholine receptors. Therefore, antimuscarinic drugs can cause anhidrosis.
Common Causes
- Miscellaneous conditions
- Symptoms and signs
- Autosomal dominant conditions
- Dermatopathia pigmentosa reticularis
- Hay-Wells syndrome
- Hereditary sensory and autonomic neuropathy type 1E
- Hypohidrotic ectodermal dysplasia, autosomal dominant
- Limb-mammary syndrome
- Marshall syndrome
- Naegeli-Franceschetti-Jadassohn syndrome
- Rapp-Hodgkin ectodermal dysplasia syndrome
- Autosomal recessive conditions
- Hereditary sensory and autonomic neuropathy type 4
- Hypohidrotic ectodermal dysplasia, autosomal recessive type
- Rosselli-Gulienetti syndrome
- X-linked inherited conditions
- Bazex-Dupre-Christol syndrome
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Hypohidrotic ectodermal dysplasia, X-linked
- Bacteria and bacterial conditions
- Iatrogenic conditions
- Sympathectomy
- Drugs, hormones and mediators
- Hexamethonium
- Topiramate
- Zonisamide
- Drug Causes