Recomendações para o Diagnóstico da Forma Tardia da Doença de Pompe

Translated title of the contribution: Diagnosis Recommendations for Late-onset Pompe Disease

Research output: Contribution to journalArticle

2 Citations (Scopus)
5 Downloads (Pure)

Abstract

Introduction: Pompe disease is a progressive and debilitating autossomal recessive myopathy due to mutations in lysossomal acid-alpha-glucosidase. Its late-onset form has a heterogeneous presentation mimicking other neuromuscular diseases, leading to diagnostic challenge. Objective: To develop consensus based recommendations for the diagnosis of late-onset Pompe Disease. Material and Methods: Bibliographic review and analysis of an opinion questionnaire applied to a group of specialists with expertise in the diagnosis of several myopathies and lysossomal storage disorders. Discussed in consensus meeting. Recommendations: Patients with a progressive limb-girdle weakness, fatigue, cramps and muscle pain should be evaluated with CK levels, electromyography, dynamic spirometry and muscle biopsy in inconclusive cases. Suspected cases and those in which muscle biopsy could not allow other diagnosis should be screened for lysossomal acid-alpha-glucosidase deficiency with DBS (dried blood spot). The diagnosis should be confirmed by determination of lysossomal acid-alpha-glucosidase activity in a second sample and lysossomal acid-alpha-glucosidase gene sequencing
Translated title of the contributionDiagnosis Recommendations for Late-onset Pompe Disease
Original languagePortuguese
Pages (from-to)525-529
Number of pages5
JournalActa medica portuguesa
Volume27
Issue number4
Publication statusPublished - Jul 2014

Fingerprint Dive into the research topics of 'Diagnosis Recommendations for Late-onset Pompe Disease'. Together they form a unique fingerprint.

Cite this