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Syndrome in question

Ross syndrome is a rare disease characterized by peripheral nervous system dysautonomia with selective degeneration of cholinergic fibers. It is composed by the triad of unilateral or bilateral segmental anhidrosis, deep hyporeflexia and Holmes-Adie's tonic pupil. The presence of compensatory s...

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Autores principales: Dalapicola, Monique Coelho, Veasey, John Verrinder, Lellis, Rute Facchini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782661/
https://www.ncbi.nlm.nih.gov/pubmed/26982793
http://dx.doi.org/10.1590/abd1806-4841.20163918
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author Dalapicola, Monique Coelho
Veasey, John Verrinder
Lellis, Rute Facchini
author_facet Dalapicola, Monique Coelho
Veasey, John Verrinder
Lellis, Rute Facchini
author_sort Dalapicola, Monique Coelho
collection PubMed
description Ross syndrome is a rare disease characterized by peripheral nervous system dysautonomia with selective degeneration of cholinergic fibers. It is composed by the triad of unilateral or bilateral segmental anhidrosis, deep hyporeflexia and Holmes-Adie's tonic pupil. The presence of compensatory sweating is frequent, usually the symptom that most afflicts patients. The aspects of the syndrome are put to discussion due to the case of a male patient, caucasian, 47 years old, with clinical onset of 25 years.
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spelling pubmed-47826612016-03-10 Syndrome in question Dalapicola, Monique Coelho Veasey, John Verrinder Lellis, Rute Facchini An Bras Dermatol Syndrome in Question Ross syndrome is a rare disease characterized by peripheral nervous system dysautonomia with selective degeneration of cholinergic fibers. It is composed by the triad of unilateral or bilateral segmental anhidrosis, deep hyporeflexia and Holmes-Adie's tonic pupil. The presence of compensatory sweating is frequent, usually the symptom that most afflicts patients. The aspects of the syndrome are put to discussion due to the case of a male patient, caucasian, 47 years old, with clinical onset of 25 years. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC4782661/ /pubmed/26982793 http://dx.doi.org/10.1590/abd1806-4841.20163918 Text en © 2016 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Syndrome in Question
Dalapicola, Monique Coelho
Veasey, John Verrinder
Lellis, Rute Facchini
Syndrome in question
title Syndrome in question
title_full Syndrome in question
title_fullStr Syndrome in question
title_full_unstemmed Syndrome in question
title_short Syndrome in question
title_sort syndrome in question
topic Syndrome in Question
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782661/
https://www.ncbi.nlm.nih.gov/pubmed/26982793
http://dx.doi.org/10.1590/abd1806-4841.20163918
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