A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.

We describe a case of the juvenile form of Pompe's disease that presented as primary alveolar hypoventilation due to respiratory muscle involvement. This 17-year-old girl had been asymptomatic until this admission, although she had a delayed puberty. Arterial blood gas analysis, pulmonary funct...

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Detalles Bibliográficos
Autores principales: Kim, D. G., Jung, K., Lee, M. K., Hyun, I. G., Lim, H. J., Song, H. G., Chi, J. G.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1993
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053741/
https://www.ncbi.nlm.nih.gov/pubmed/8240754
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author Kim, D. G.
Jung, K.
Lee, M. K.
Hyun, I. G.
Lim, H. J.
Song, H. G.
Chi, J. G.
author_facet Kim, D. G.
Jung, K.
Lee, M. K.
Hyun, I. G.
Lim, H. J.
Song, H. G.
Chi, J. G.
author_sort Kim, D. G.
collection PubMed
description We describe a case of the juvenile form of Pompe's disease that presented as primary alveolar hypoventilation due to respiratory muscle involvement. This 17-year-old girl had been asymptomatic until this admission, although she had a delayed puberty. Arterial blood gas analysis, pulmonary function test as well as physical findings were compatible with chronic alveolar hypoventilation syndrome. Since she had lower extremity muscle weakness and pseudomyotonic discharge on electromyography a muscle biopsy was done, which revealed glycogen storage disease. The patient was managed successfully with nasal intermittent positive pressure ventilation.
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spelling pubmed-30537412011-03-16 A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation. Kim, D. G. Jung, K. Lee, M. K. Hyun, I. G. Lim, H. J. Song, H. G. Chi, J. G. J Korean Med Sci Research Article We describe a case of the juvenile form of Pompe's disease that presented as primary alveolar hypoventilation due to respiratory muscle involvement. This 17-year-old girl had been asymptomatic until this admission, although she had a delayed puberty. Arterial blood gas analysis, pulmonary function test as well as physical findings were compatible with chronic alveolar hypoventilation syndrome. Since she had lower extremity muscle weakness and pseudomyotonic discharge on electromyography a muscle biopsy was done, which revealed glycogen storage disease. The patient was managed successfully with nasal intermittent positive pressure ventilation. Korean Academy of Medical Sciences 1993-06 /pmc/articles/PMC3053741/ /pubmed/8240754 Text en
spellingShingle Research Article
Kim, D. G.
Jung, K.
Lee, M. K.
Hyun, I. G.
Lim, H. J.
Song, H. G.
Chi, J. G.
A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.
title A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.
title_full A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.
title_fullStr A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.
title_full_unstemmed A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.
title_short A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation.
title_sort case of juvenile form pompe's disease manifested as chronic alveolar hypoventilation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053741/
https://www.ncbi.nlm.nih.gov/pubmed/8240754
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