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Nodding syndrome- an Indian case

BACKGROUND: Although nodding syndrome is a catastrophic epileptic encephalopathy, it is reported only from Africa so far. We describe the first case from the Indian sub-continent. METHODS: A ten-year-old child who had an episode of Guillain Barre syndrome with incomplete recovery developed emaciatio...

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Autores principales: Sehgal, Rachna, Agarwal, Neha, Gera, Rani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Makerere Medical School 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306992/
https://www.ncbi.nlm.nih.gov/pubmed/30603018
http://dx.doi.org/10.4314/ahs.v18i3.43
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author Sehgal, Rachna
Agarwal, Neha
Gera, Rani
author_facet Sehgal, Rachna
Agarwal, Neha
Gera, Rani
author_sort Sehgal, Rachna
collection PubMed
description BACKGROUND: Although nodding syndrome is a catastrophic epileptic encephalopathy, it is reported only from Africa so far. We describe the first case from the Indian sub-continent. METHODS: A ten-year-old child who had an episode of Guillain Barre syndrome with incomplete recovery developed emaciation secondary to bulbar palsy and depression. Subsequently, nine months later she developed head nodding, spastic quadriparesis, choreo-athetoid movement disorder, global aphasia and depression. She improved with sodium valproate, nutritional rehabilitation and anti-spasticity and anti-depressant medications. RESULTS: First case of nodding syndrome is described from India where possible etiology is malnutrition. She had anemia, her electroencephalography revealed parieto-occipital inter-ictal epileptiform discharges and Magnetic Resonance Imaging showed diffuse cerebral atrophy. CONCLUSION: Nodding syndrome is an epileptic encephalopathy of nutritional origin beyond geographical barriers but amenable to anti-convulsants and nutritional rehabilitation.
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spelling pubmed-63069922019-01-02 Nodding syndrome- an Indian case Sehgal, Rachna Agarwal, Neha Gera, Rani Afr Health Sci Articles BACKGROUND: Although nodding syndrome is a catastrophic epileptic encephalopathy, it is reported only from Africa so far. We describe the first case from the Indian sub-continent. METHODS: A ten-year-old child who had an episode of Guillain Barre syndrome with incomplete recovery developed emaciation secondary to bulbar palsy and depression. Subsequently, nine months later she developed head nodding, spastic quadriparesis, choreo-athetoid movement disorder, global aphasia and depression. She improved with sodium valproate, nutritional rehabilitation and anti-spasticity and anti-depressant medications. RESULTS: First case of nodding syndrome is described from India where possible etiology is malnutrition. She had anemia, her electroencephalography revealed parieto-occipital inter-ictal epileptiform discharges and Magnetic Resonance Imaging showed diffuse cerebral atrophy. CONCLUSION: Nodding syndrome is an epileptic encephalopathy of nutritional origin beyond geographical barriers but amenable to anti-convulsants and nutritional rehabilitation. Makerere Medical School 2018-09 /pmc/articles/PMC6306992/ /pubmed/30603018 http://dx.doi.org/10.4314/ahs.v18i3.43 Text en © 2018 Sehgal et al. Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Sehgal, Rachna
Agarwal, Neha
Gera, Rani
Nodding syndrome- an Indian case
title Nodding syndrome- an Indian case
title_full Nodding syndrome- an Indian case
title_fullStr Nodding syndrome- an Indian case
title_full_unstemmed Nodding syndrome- an Indian case
title_short Nodding syndrome- an Indian case
title_sort nodding syndrome- an indian case
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306992/
https://www.ncbi.nlm.nih.gov/pubmed/30603018
http://dx.doi.org/10.4314/ahs.v18i3.43
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