Literature DB >> 267557

Adult-onset acid maltase deficiency. Case report of an adult with severe respiratory difficulty.

N I Lightman, R T Schooley.   

Abstract

Pompe's disease (acid maltase deficiency) classically affects infants and children, with a few sporadic cases occurring in adults. An adult patient initially have progressive muscular weakness, exertional dyspnea, diaphragmatic paralysis, and objective evidence of restrictive respiratory disease. Muscle biopsy established the diagnosis of acid maltase deficiency. The patient's brother had died at the age of 44 years, after 23 years of a "progressive muscular dystrophy." Acid maltase deficiency should be considered in the differential diagnosis of progressive respiratory insufficiency associated with weakness.

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Year:  1977        PMID: 267557     DOI: 10.1378/chest.72.2.250

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  3 in total

Review 1.  The natural course of non-classic Pompe's disease; a review of 225 published cases.

Authors:  Léon P F Winkel; Marloes L C Hagemans; Pieter A van Doorn; M Christa B Loonen; Wim J C Hop; Arnold J J Reuser; Ans T van der Ploeg
Journal:  J Neurol       Date:  2005-08       Impact factor: 4.849

2.  Respiratory failure as initial symptom of acid maltase deficiency.

Authors:  R W Keunen; P C Lambregts; A A Op de Coul; E M Joosten
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-05       Impact factor: 10.154

3.  Respiratory muscle and pulmonary function in polymyositis and other proximal myopathies.

Authors:  N M Braun; N S Arora; D F Rochester
Journal:  Thorax       Date:  1983-08       Impact factor: 9.139

  3 in total

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