Hypohidrosis

"Hypohidrosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Abnormally diminished or absent perspiration. Both generalized and segmented (reduced or absent sweating in circumscribed locations) forms of the disease are usually associated with other underlying conditions.

Descriptor ID

D007007

MeSH Number(s)

C17.800.946.370

Concept/Terms

Hypohidrosis

Anhidrosis

Below are MeSH descriptors whose meaning is more general than "Hypohidrosis".

Diseases [C]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Sweat Gland Diseases [C17.800.946]
Hypohidrosis [C17.800.946.370]

Below are MeSH descriptors whose meaning is related to "Hypohidrosis".

Below are MeSH descriptors whose meaning is more specific than "Hypohidrosis".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Hypohidrosis" by people in Harvard Catalyst Profiles by year, and whether "Hypohidrosis" was a major or minor topic of these publication.

Bar chart showing 17 publications over 11 distinct years, with a maximum of 3 publications in 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1998	1	1	2
2002	2	0	2
2009	0	1	1
2013	1	0	1
2014	1	0	1
2015	2	0	2
2016	2	0	2
2019	0	1	1
2021	3	0	3
2022	1	0	1
2023	1	0	1

Below are the most recent publications written about "Hypohidrosis" by people in Profiles.

Clinical and molecular features of four families with CLDN10-related HELIX syndrome. Eur J Med Genet. 2023 Dec; 66(12):104886.

View in: PubMed
Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF ?B-Mediated Autoinflammatory Disease with Retinal Dystrophy. Ophthalmology. 2023 04; 130(4):423-432.

View in: PubMed
Structural analysis of TrkA mutations in patients with congenital insensitivity to pain reveals PLC? as an analgesic drug target. Sci Signal. 2022 04 26; 15(731):eabm6046.

View in: PubMed
Beneficial screening of Fabry disease in patients with hypohidrosis. J Dermatol. 2022 Feb; 49(2):308-312.

View in: PubMed
Harlequin Syndrome, Apnea, and Acute on Chronic Hemiparesis: An Atypical Pediatric Case of Chiari I With Holocord Syringohydromyelia. Pediatr Neurol. 2022 01; 126:108-109.

View in: PubMed
Neuropsychological Profile of an Adolescent Female With Ectodermal Dysplasia With Hypohidrosis. Cogn Behav Neurol. 2021 09 02; 34(3):212-219.

View in: PubMed
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder. Genet Med. 2019 09; 21(9):2103-2115.

View in: PubMed
Harlequin Syndrome Associated with Multilevel Intercostal Nerve Block. Anesthesiology. 2016 Nov; 125(5):1045.

View in: PubMed
Congenital insensitivity to pain and anhidrosis: Case report and review of findings along neuro-immune axis in the disorder. J Neurol Sci. 2016 Nov 15; 370:201-210.

View in: PubMed
Harlequin Syndrome After Thoracic Paravertebral Block. A A Case Rep. 2016 Feb 01; 6(3):48-51.

View in: PubMed

Related Networks

People

Explore

Similar Concepts

Top Journals

J Med Genet
J Am Acad Dermatol
Headache
Harefuah
Eur J Med Genet
Cogn Behav Neurol
Anesthesiology
Am J Ophthalmol
Am J Med Genet A
A A Case Rep