Open AccessReport of the first Brazilian infantile Pompe disease patient to be treated with recombinant human acid alpha-glucosidase
Author(s) -
Sandra J. Pereira,
C eacute lia R. Berditchevisky
Publication year - 2008
Publication title -
jornal de pediatria
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.645
H-Index - 52
eISSN - 1678-4782
pISSN - 0021-7557
DOI - 10.2223/jped.1793
Subject(s) - medicine , hypotonia , glycogen storage disease type ii , disease , enzyme replacement therapy , pediatrics , glycogen storage disease , girl , glycogen , hypertrophic cardiomyopathy , respiratory failure , incidence (geometry) , psychology , developmental psychology , physics , optics
To describe the first case of infantile Pompe disease to be treated in Brazil.
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