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The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire)
The Kleine-Levin syndrome is a rare pathology characterized by recurrent episodes of hypersomnia associated with behavioral and cognitive disorders with, among others, hyperphagia and hypersexuality. The disease mainly affects young males. A few studies mention cases that occurred in Africa, especia...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773539/ https://www.ncbi.nlm.nih.gov/pubmed/26989535 http://dx.doi.org/10.1155/2016/8929413 |
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author | Assi, Berthe Yapo-Ehounoud, Constance Baby, Mohamed Ben Allaoui Aka-Diarra, Evelyne Amon-Tanoh, Muriel Tanoh, Christian |
author_facet | Assi, Berthe Yapo-Ehounoud, Constance Baby, Mohamed Ben Allaoui Aka-Diarra, Evelyne Amon-Tanoh, Muriel Tanoh, Christian |
author_sort | Assi, Berthe |
collection | PubMed |
description | The Kleine-Levin syndrome is a rare pathology characterized by recurrent episodes of hypersomnia associated with behavioral and cognitive disorders with, among others, hyperphagia and hypersexuality. The disease mainly affects young males. A few studies mention cases that occurred in Africa, especially in Côte d'Ivoire. In this paper, we report the very first two cases observed in the Neurology Department of the University Hospital of Cocody. The diagnosis was clinical, based on the recurrence of hypersomnia, cognitive and behavioral disorders during the periods of hypersomnia, and the return of patients to normal state between episodes. This diagnosis was delayed due to failure to understand the pathology, thereby leading patients to wandering. In fact, the two patients were consulted, respectively, 3 years and 6 years after the hypersomnia began. The objective was to report the very first cases observed in the Neurology Department of the University Hospital of Cocody, Côte d'Ivoire. |
format | Online Article Text |
id | pubmed-4773539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47735392016-03-17 The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) Assi, Berthe Yapo-Ehounoud, Constance Baby, Mohamed Ben Allaoui Aka-Diarra, Evelyne Amon-Tanoh, Muriel Tanoh, Christian Case Rep Neurol Med Case Report The Kleine-Levin syndrome is a rare pathology characterized by recurrent episodes of hypersomnia associated with behavioral and cognitive disorders with, among others, hyperphagia and hypersexuality. The disease mainly affects young males. A few studies mention cases that occurred in Africa, especially in Côte d'Ivoire. In this paper, we report the very first two cases observed in the Neurology Department of the University Hospital of Cocody. The diagnosis was clinical, based on the recurrence of hypersomnia, cognitive and behavioral disorders during the periods of hypersomnia, and the return of patients to normal state between episodes. This diagnosis was delayed due to failure to understand the pathology, thereby leading patients to wandering. In fact, the two patients were consulted, respectively, 3 years and 6 years after the hypersomnia began. The objective was to report the very first cases observed in the Neurology Department of the University Hospital of Cocody, Côte d'Ivoire. Hindawi Publishing Corporation 2016 2016-02-17 /pmc/articles/PMC4773539/ /pubmed/26989535 http://dx.doi.org/10.1155/2016/8929413 Text en Copyright © 2016 Berthe Assi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Assi, Berthe Yapo-Ehounoud, Constance Baby, Mohamed Ben Allaoui Aka-Diarra, Evelyne Amon-Tanoh, Muriel Tanoh, Christian The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) |
title | The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) |
title_full | The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) |
title_fullStr | The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) |
title_full_unstemmed | The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) |
title_short | The Kleine-Levin Syndrome: A Rare Disease with Often Delayed Diagnosis—A Report of Two Cases in the Department of Neurology of the University Hospital of Cocody (Côte d'Ivoire) |
title_sort | kleine-levin syndrome: a rare disease with often delayed diagnosis—a report of two cases in the department of neurology of the university hospital of cocody (côte d'ivoire) |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773539/ https://www.ncbi.nlm.nih.gov/pubmed/26989535 http://dx.doi.org/10.1155/2016/8929413 |
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