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An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty

Infants with Sandhoff disease typically appear normal until 3–6 months of age. As the disease progresses, they present with symptoms such as loss of motor skills, exaggerated startle response to loud noise, seizures, visual loss, and paralysis. We encountered a rare case of a 22-month-old girl with...

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Autores principales: Moon, Jae-Gun, Shin, Min-A, Pyo, Hannah, Choi, Seong-Uk, Kim, Hyun-Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Rehabilitation Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698679/
https://www.ncbi.nlm.nih.gov/pubmed/29201831
http://dx.doi.org/10.5535/arm.2017.41.5.892
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author Moon, Jae-Gun
Shin, Min-A
Pyo, Hannah
Choi, Seong-Uk
Kim, Hyun-Kyung
author_facet Moon, Jae-Gun
Shin, Min-A
Pyo, Hannah
Choi, Seong-Uk
Kim, Hyun-Kyung
author_sort Moon, Jae-Gun
collection PubMed
description Infants with Sandhoff disease typically appear normal until 3–6 months of age. As the disease progresses, they present with symptoms such as loss of motor skills, exaggerated startle response to loud noise, seizures, visual loss, and paralysis. We encountered a rare case of a 22-month-old girl with Sandhoff disease characterized by progressive motor weakness and dysphagia, who initially showed signs of aspiration at 20 months of age. The major problems related to dysphagia were oromotor dysfunction and abnormal feeding posture. Within 3 months of identification of difficulty in swallowing, the patient showed a significant decrease in food intake, with rapid deterioration of nutritional status. We report our case with a review of the literature.
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spelling pubmed-56986792017-12-03 An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty Moon, Jae-Gun Shin, Min-A Pyo, Hannah Choi, Seong-Uk Kim, Hyun-Kyung Ann Rehabil Med Case Report Infants with Sandhoff disease typically appear normal until 3–6 months of age. As the disease progresses, they present with symptoms such as loss of motor skills, exaggerated startle response to loud noise, seizures, visual loss, and paralysis. We encountered a rare case of a 22-month-old girl with Sandhoff disease characterized by progressive motor weakness and dysphagia, who initially showed signs of aspiration at 20 months of age. The major problems related to dysphagia were oromotor dysfunction and abnormal feeding posture. Within 3 months of identification of difficulty in swallowing, the patient showed a significant decrease in food intake, with rapid deterioration of nutritional status. We report our case with a review of the literature. Korean Academy of Rehabilitation Medicine 2017-10 2017-10-31 /pmc/articles/PMC5698679/ /pubmed/29201831 http://dx.doi.org/10.5535/arm.2017.41.5.892 Text en Copyright © 2017 by Korean Academy of Rehabilitation Medicine 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 (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Moon, Jae-Gun
Shin, Min-A
Pyo, Hannah
Choi, Seong-Uk
Kim, Hyun-Kyung
An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty
title An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty
title_full An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty
title_fullStr An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty
title_full_unstemmed An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty
title_short An Infantile Case of Sandhoff Disease Presenting With Swallowing Difficulty
title_sort infantile case of sandhoff disease presenting with swallowing difficulty
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698679/
https://www.ncbi.nlm.nih.gov/pubmed/29201831
http://dx.doi.org/10.5535/arm.2017.41.5.892
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