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Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome
Nakalanga syndrome is a condition that was described in Uganda and various other African countries decades ago. Its features include growth retardation, physical deformities, endocrine dysfunction, mental impairment, and epilepsy, amongst others. Its cause remains obscure. Nodding syndrome is a neur...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300103/ https://www.ncbi.nlm.nih.gov/pubmed/28182652 http://dx.doi.org/10.1371/journal.pntd.0005201 |
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author | Föger, Kathrin Gora-Stahlberg, Gina Sejvar, James Ovuga, Emilio Jilek-Aall, Louise Schmutzhard, Erich Kaiser, Christoph Winkler, Andrea S. |
author_facet | Föger, Kathrin Gora-Stahlberg, Gina Sejvar, James Ovuga, Emilio Jilek-Aall, Louise Schmutzhard, Erich Kaiser, Christoph Winkler, Andrea S. |
author_sort | Föger, Kathrin |
collection | PubMed |
description | Nakalanga syndrome is a condition that was described in Uganda and various other African countries decades ago. Its features include growth retardation, physical deformities, endocrine dysfunction, mental impairment, and epilepsy, amongst others. Its cause remains obscure. Nodding syndrome is a neurological disorder with some features in common with Nakalanga syndrome, which has been described mainly in Uganda, South Sudan, and Tanzania. It has been considered an encephalopathy affecting children who, besides head nodding attacks, can also present with stunted growth, delayed puberty, and mental impairment, amongst other symptoms. Despite active research over the last years on the pathogenesis of Nodding syndrome, to date, no convincing single cause of Nodding syndrome has been reported. In this review, by means of a thorough literature search, we compare features of both disorders. We conclude that Nakalanga and Nodding syndromes are closely related and may represent the same condition. Our findings may provide new directions in research on the cause underlying this neurological disorder. |
format | Online Article Text |
id | pubmed-5300103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53001032017-02-28 Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome Föger, Kathrin Gora-Stahlberg, Gina Sejvar, James Ovuga, Emilio Jilek-Aall, Louise Schmutzhard, Erich Kaiser, Christoph Winkler, Andrea S. PLoS Negl Trop Dis Review Nakalanga syndrome is a condition that was described in Uganda and various other African countries decades ago. Its features include growth retardation, physical deformities, endocrine dysfunction, mental impairment, and epilepsy, amongst others. Its cause remains obscure. Nodding syndrome is a neurological disorder with some features in common with Nakalanga syndrome, which has been described mainly in Uganda, South Sudan, and Tanzania. It has been considered an encephalopathy affecting children who, besides head nodding attacks, can also present with stunted growth, delayed puberty, and mental impairment, amongst other symptoms. Despite active research over the last years on the pathogenesis of Nodding syndrome, to date, no convincing single cause of Nodding syndrome has been reported. In this review, by means of a thorough literature search, we compare features of both disorders. We conclude that Nakalanga and Nodding syndromes are closely related and may represent the same condition. Our findings may provide new directions in research on the cause underlying this neurological disorder. Public Library of Science 2017-02-09 /pmc/articles/PMC5300103/ /pubmed/28182652 http://dx.doi.org/10.1371/journal.pntd.0005201 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Review Föger, Kathrin Gora-Stahlberg, Gina Sejvar, James Ovuga, Emilio Jilek-Aall, Louise Schmutzhard, Erich Kaiser, Christoph Winkler, Andrea S. Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome |
title | Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome |
title_full | Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome |
title_fullStr | Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome |
title_full_unstemmed | Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome |
title_short | Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome |
title_sort | nakalanga syndrome: clinical characteristics, potential causes, and its relationship with recently described nodding syndrome |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5300103/ https://www.ncbi.nlm.nih.gov/pubmed/28182652 http://dx.doi.org/10.1371/journal.pntd.0005201 |
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