Literature DB >> 23486339

Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes.

Jun Kido1, Kimitoshi Nakamura, Shirou Matsumoto, Hiroshi Mitsubuchi, Toshihiro Ohura, Yosuke Shigematsu, Tohru Yorifuji, Mureo Kasahara, Reiko Horikawa, Fumio Endo.   

Abstract

Many reports have been published on the long-term outcome and treatment of hepatic glycogen storage diseases (GSDs) overseas; however, none have been published from Japan. We investigated the clinical manifestations, treatment, and prognosis of 127 hepatic GSD patients who were evaluated and treated between January 1999 and December 2009. A characteristic genetic pattern was noted in the Japanese GSD patients: most GSD Ia patients had the g727t mutation, and many GSD Ib patients had the W118R mutation. Forty-one percent (14/34) of GSD Ia patients and 18% (2/11) of GSD Ib patients of ages 13 years 4 months had liver adenoma. Among subjects aged 10 years, 19% (7/36) of the GSD Ia patients and none of the GSD Ib patients had renal dysfunction. The mean height of male GSD Ia patients aged 18 years was 160.8±10.6 cm (n=14), and that of their female counterparts was 147.8±3.80 cm (n=9). Patients with hepatic GSDs develop a variety of symptoms but can survive in the long term by diet therapy, corn starch treatment and supportive care. Liver transplantation for hepatic GSDs is an important treatment strategy and can help improve the patients'quality of life.

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Year:  2013        PMID: 23486339     DOI: 10.1038/jhg.2013.17

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  9 in total

1.  Clinical and Molecular Variability in Patients with PHKA2 Variants and Liver Phosphorylase b Kinase Deficiency.

Authors:  Deeksha S Bali; Jennifer L Goldstein; Keri Fredrickson; Stephanie Austin; Surekha Pendyal; Catherine Rehder; Priya S Kishnani
Journal:  JIMD Rep       Date:  2017-03-12

2.  Molecular analysis of glycogen storage disease type Ia in Iranian Azeri Turks: identification of a novel mutation.

Authors:  Shekari Khaniani Mahmoud; Aziz Khorrami; Mandana Rafeey; Robabeh Ghergherehchi; Mansoori Derakhshan Sima
Journal:  J Genet       Date:  2017-03       Impact factor: 1.166

Review 3.  Molecular biology and gene therapy for glycogen storage disease type Ib.

Authors:  Janice Y Chou; Jun-Ho Cho; Goo-Young Kim; Brian C Mansfield
Journal:  J Inherit Metab Dis       Date:  2018-04-16       Impact factor: 4.982

Review 4.  The Phenotypic and Genetic Spectrum of Glycogen Storage Disease Type VI.

Authors:  Sarah Catharina Grünert; Luciana Hannibal; Ute Spiekerkoetter
Journal:  Genes (Basel)       Date:  2021-08-03       Impact factor: 4.096

5.  Quality of life in adult patients with glycogen storage disease type I: results of a multicenter italian study.

Authors:  Annalisa Sechi; Laura Deroma; Sabrina Paci; Annunziata Lapolla; Francesca Carubbi; Alberto Burlina; Miriam Rigoldi; Maja Di Rocco
Journal:  JIMD Rep       Date:  2013-12-21

6.  Clinical manifestations and growth of patients with urea cycle disorders in Japan.

Authors:  Kimitoshi Nakamura; Jun Kido; Shirou Matsumoto; Hiroshi Mitsubuchi; Fumio Endo
Journal:  J Hum Genet       Date:  2016-03-03       Impact factor: 3.172

7.  Does type I truly dominate hepatic glycogen storage diseases in Korea?: a single center study.

Authors:  Yu Ju Jeong; Ben Kang; So Yoon Choi; Chang-Seok Ki; Soo-Youn Lee; Hyung-Doo Park; Yon Ho Choe
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2014-12-31

8.  A novel SLC37A4 missense mutation in GSD-Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosis.

Authors:  Qianyun Xu; Haiyan Tang; Liping Duan; Xiaoxia Zuo; Xiaoliu Shi; Yisha Li; Hongjun Zhao; Huali Zhang
Journal:  Mol Genet Genomic Med       Date:  2020-12-05       Impact factor: 2.183

9.  Predominance of the c.648G > T G6PC gene mutation and late complications in Korean patients with glycogen storage disease type Ia.

Authors:  Yoo-Mi Kim; Jin-Ho Choi; Beom-Hee Lee; Gu-Hwan Kim; Kyung-Mo Kim; Han-Wook Yoo
Journal:  Orphanet J Rare Dis       Date:  2020-02-11       Impact factor: 4.123

  9 in total

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