Literature DB >> 18092126

Glycogen storage disease manifested as gout and myopathy: three case reports and literature review.

Wei Zhang1, Chun-de Bao, Yue-ying Gu, Shuang Ye.   

Abstract

Glycogen storage diseases (GSDs) are a group of congenital inherited metabolic diseases. They may present the symptoms of muscle and joint which may be misdiagnosed with some rheumatic diseases. We report three cases of GSDs in order to have a more clear recognition of the disease and to discuss the differential diagnosis.

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Year:  2007        PMID： 18092126     DOI： 10.1007/s10067-007-0798-4

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN： 0770-3198            Impact factor:   2.980


  6 in total

Review 1.  Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families.

Authors:  M G Ausems; K ten Berg; F A Beemer; J H Wokke
Journal:  Neuromuscul Disord       Date:  2000-10       Impact factor: 4.296

2.  A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease.

Authors:  Priya S Kishnani; Wuh-Liang Hwu; Hanna Mandel; Marc Nicolino; Florence Yong; Deyanira Corzo
Journal:  J Pediatr       Date:  2006-05       Impact factor: 4.406

Review 3.  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

Review 4.  Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.

Authors:  Janice Yang Chou; Dietrich Matern; Brian C Mansfield; Yuan-Tsong Chen
Journal:  Curr Mol Med       Date:  2002-03       Impact factor: 2.222

5.  Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease.

Authors:  Priya Sunil Kishnani; Marc Nicolino; Thomas Voit; R Curtis Rogers; Anne Chun-Hui Tsai; John Waterson; Gail E Herman; Andreas Amalfitano; Beth L Thurberg; Susan Richards; Mark Davison; Deyanira Corzo; Y T Chen
Journal:  J Pediatr       Date:  2006-07       Impact factor: 4.406

6.  Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk.

Authors:  Johanna M P Van den Hout; Joep H J Kamphoven; Léon P F Winkel; Willem F M Arts; Johannes B C De Klerk; M Christa B Loonen; Arnold G Vulto; Adri Cromme-Dijkhuis; Nynke Weisglas-Kuperus; Wim Hop; Hans Van Hirtum; Otto P Van Diggelen; Marijke Boer; Marian A Kroos; Pieter A Van Doorn; Edwin Van der Voort; Barbara Sibbles; Emiel J J M Van Corven; Just P J Brakenhoff; Johan Van Hove; Jan A M Smeitink; Gerard de Jong; Arnold J J Reuser; Ans T Van der Ploeg
Journal:  Pediatrics       Date:  2004-05       Impact factor: 7.124
  6 in total
  3 in total

Review 1.  Hyperuricemia in Children and Adolescents: Present Knowledge and Future Directions.

Authors:  Masaru Kubota
Journal:  J Nutr Metab       Date:  2019-05-02

Review 2.  Clinical features of gout in adult patients with type Ia glycogen storage disease: a single-centre retrospective study and a review of literature.

Authors:  Na Xu; Xinxin Han; Yun Zhang; Xiaoming Huang; Weiguo Zhu; Min Shen; Wen Zhang; Chen Jialin; Min Wei; Zhengqing Qiu; Xuejun Zeng
Journal:  Arthritis Res Ther       Date:  2022-02-26       Impact factor: 5.156

Review 3.  Tophaceous gout in a female premenopausal patient with an unexpected diagnosis of glycogen storage disease type Ia: a case report and literature review.

Authors:  Bingqing Zhang; Xuejun Zeng
Journal:  Clin Rheumatol       Date:  2016-05-02       Impact factor: 2.980
  3 in total

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