A Case of Adult-onset Pompe Disease with Cerebral Stroke and Left Ventricular Hypertrophy

Author:

Hossain Mohammad ArifORCID,Miyajima Takashi,Akiyama Keiko,Eto Yoshikatsu

Funder

Ministry of Education, Culture, Science, Sports and Technology

Ministry of Health, Labor and Welfare of Japan

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Rehabilitation,Surgery

Reference22 articles.

1. Glycogen storage disease type II: acid α-glucosidase (acid maltase) deficiency;Hirschhorn,2013

2. Acid maltase deficiency: comparison of infantile, childhood, and adult types;Engel;Neurology,1970

3. Pompe disease: a neuromuscular disease with respiratory muscle involvement;Mellies;Respir Med,2009

4. The emerging phenotype of late-onset Pompe disease: a systematic literature review;Chan;Mol Genet Metab,2017

5. Adult onset acid maltase deficiency. Distribution and progression of clinical and pathological abnormality in a family;Swash;J Neurol Sci,1985

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