Clinical Variability in 2 Siblings With Late-Onset Pompe Disease
J Clin Neuromuscul Dis
.
2018 Sep;20(1):47-48.
doi: 10.1097/CND.0000000000000216.
Authors
Carolina da Cunha Correia
1
,
Pedro Nogueira Fontana
1
,
Gustavo Henrique Belarmino de Góes
1
,
Edmar Zanoteli
2
Affiliations
1
Departamento de Neurologia, Hospital Universitário Oswaldo Cruz, Universidade de Pernambuco, Recife, Brazil.
2
Departamento de Neurologia, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, Brazil.
PMID:
30124561
DOI:
10.1097/CND.0000000000000216
No abstract available
Publication types
Case Reports
MeSH terms
Adult
Glycogen Storage Disease Type II / genetics
Glycogen Storage Disease Type II / metabolism*
Humans
Male
Middle Aged
Siblings*
alpha-Glucosidases / genetics
alpha-Glucosidases / metabolism
Substances
alpha-Glucosidases