Homozygotic intronic GAA mutation in three siblings with late-onset Pompe's disease

• Autor(a) principal: Grzesiuk, Anderson Kuntz
• Data de Publicação: 2010
• Outros Autores: Shinjo, Sueli Mieko Oba, Silva, Roseli da, Machado, Marcela [UNIFESP], Galera, Marcial Francis [UNIFESP], Marie, Suely Kazue Nagahashi
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• Texto Completo: http://dx.doi.org/10.1590/S0004-282X2010000200008; http://repositorio.unifesp.br/handle/11600/5678
• topic: glycogen storage disease type II; mutation; Pompe disease; doença de Pompe; mutação; glicogenose

Pompe's disease (PD) is a metabolic myopathy caused by the accumulation of lysosomal glycogen, secondary to acid α-glucosidase (GAA) enzyme deficiency. Childhood and late-onset forms are described, differing by the age of onset and symptoms. In this study were analyzed affected siblings with Pompe's disease (PD) and their distinct clinical and pathological presentations. METHOD: Diagnosis was performed by the clinical presentation of limb-girdle dystrophies and respiratory compromise. Confirmatory diagnoses were conducted by muscle biopsy, GAA activity measurement and by GAA gene genotyping. RESULTS: The findings suggested muscular involvement due to GAA deficiency. GAA genotyping showed they are homozygous for the c.-32-3C>A mutation. CONCLUSION: Herein we reported a family where three out of five siblings were diagnosed with late-onset PD, although it is a rare metabolic disease inherited in an autossomal recessive manner. We emphasize the importance of including this presentation within the differential diagnoses of the limb-girdle dystrophies once enzyme replacement therapy is available.