GM1 Gangliosidosis Type 1 and Mongolian Spots
DOI:
https://doi.org/10.15844/pedneurbriefs-27-6-10Keywords:
Hepatosplenomegaly, GM1 Gangliosidosis Type 1, Lysosomal DiseaseAbstract
Investigators in Sao Paulo, Brazil, report a female infant born at term to healthy consanguineous parents who was examined at 9 months for delayed development.Published
2013-06-01
Issue
Section
Neuromuscular Disorders
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