JUVENILE POMPE

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TONEKABONI SEYYED HASSAN

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Journal Paper

Paper Information

Journal: Iranian Journal of Child Neurology Year:2012 | Volume:6 | Issue:4 (SUPPL 1) Page(s): 10-10

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Information Journal Paper

Title

JUVENILE POMPE

Author(s)

TONEKABONI SEYYED HASSAN | Issue Writer Certificate

Keywords

CHILD

ACID MALTASE DEFICIENCY

MUSCLE WEAKNESS

Abstract

Pompe disease (Acid Maltase deficiency) has been traditionally classified into 3 forms: infantile, CHILDhood and adult. But in fact Patients are distributed in a spectrum of signs and symptoms between severe and lethal infantile form to adult type with minor problem in CHILDhood and mild progressive muscular weakness.Some authorities use “CHILDhood” or “Juvenile” pompe in view of CHILD’s age at the beginning of the first clinical manifestations. Others utilize this term to specify patients without cardiomyopathy and with exclusive skeletal muscle involvement.

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APA: Copy

TONEKABONI, SEYYED HASSAN. (2012). JUVENILE POMPE. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 6(4 (SUPPL 1)), 10-10. SID. https://sid.ir/paper/303460/en

Vancouver: Copy

TONEKABONI SEYYED HASSAN. JUVENILE POMPE. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2012;6(4 (SUPPL 1)):10-10. Available from: https://sid.ir/paper/303460/en

IEEE: Copy

SEYYED HASSAN TONEKABONI, “JUVENILE POMPE,” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 6, no. 4 (SUPPL 1), pp. 10–10, 2012, [Online]. Available: https://sid.ir/paper/303460/en

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