Literature DB >> 18301443

p.[G576S; E689K]: pathogenic combination or polymorphism in Pompe disease?

Marian A Kroos1, Reinier A Mullaart, Laura Van Vliet, Robert J Pomponio, Hernan Amartino, Edwin H Kolodny, Gregory M Pastores, Ron A Wevers, Ans T Van der Ploeg, Dicky J J Halley, Arnold J J Reuser.   

Abstract

We discuss four cases of acid alpha-glucosidase deficiency (EC, 3.2.1.3/20) without evident symptoms of Pompe disease (OMIM No 232300) in individuals of Asian descent. In three cases, the deficiency was associated with homozygosity for the sequence variant c.[1726G>A; 2065G>A] in the acid alpha-glucosidase gene (GAA) translating into p.[G576S; E689K]. One of these cases was a patient with profound muscular atrophy, another had cardio-myopathy and the third had no symptoms. The fourth case, the mother of a child with Pompe disease, was compound heterozygote for the GAA sequence variants c.[1726G>A; 2065G>A]/c.2338G>A (p.W746X) and had no symptoms either. Further investigations revealed that c.[1726A; 2065A] is a common GAA allele in the Japanese and Chinese populations. Our limited study predicts that approximately 4% of individuals in these populations are homozygote c.[1726A; 2065A]. The height of this figure in contrast to the rarity of Pompe disease in Asian populations and the clinical history of the cases described in this paper virtually exclude that homozygosity for c.[1726A; 2065A] causes Pompe disease. As c.[1726A; 2065A] homozygotes have been observed with similarly low acid alpha-glucosidase activity as some patients with Pompe disease, we caution they may present as false positives in newborn screening programs especially in Asian populations.

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Year:  2008        PMID: 18301443     DOI: 10.1038/ejhg.2008.34

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  16 in total

1.  Liquid Chromatography-Tandem Mass Spectrometry Assay of Leukocyte Acid α-Glucosidase for Post-Newborn Screening Evaluation of Pompe Disease.

Authors:  Na Lin; Jingyu Huang; Sara Violante; Joseph J Orsini; Michele Caggana; Erin E Hughes; Colleen Stevens; Lisa DiAntonio; Hsuan Chieh Liao; Xinying Hong; Farideh Ghomashchi; Arun Babu Kumar; Hui Zhou; Ruth Kornreich; Melissa Wasserstein; Michael H Gelb; Chunli Yu
Journal:  Clin Chem       Date:  2017-02-14       Impact factor: 8.327

Review 2.  Newborn screening: Taiwanese experience.

Authors:  Yin-Hsiu Chien; Wuh-Liang Hwu; Ni-Chung Lee
Journal:  Ann Transl Med       Date:  2019-07

3.  Baseline Urinary Glucose Tetrasaccharide Concentrations in Patients with Infantile- and Late-Onset Pompe Disease Identified by Newborn Screening.

Authors:  Yin-Hsiu Chien; Jennifer L Goldstein; Wuh-Liang Hwu; P Brian Smith; Ni-Chung Lee; Shu-Chuan Chiang; Adviye A Tolun; Haoyue Zhang; Amie E Vaisnins; David S Millington; Priya S Kishnani; Sarah P Young
Journal:  JIMD Rep       Date:  2015-02-15

4.  Duchenne Muscular Dystrophy With Low Acidic α-Glucosidase Activity: Two Case Reports and Literature Review.

Authors:  Xiufang He; Xuandi Li; Yuese Lin; Hongjun Ba; Huimin Peng; Lili Zhang; Ling Zhu; Youzhen Qin; Shujuan Li
Journal:  Front Pediatr       Date:  2022-06-01       Impact factor: 3.569

Review 5.  Pompe disease: literature review and case series.

Authors:  Majed Dasouki; Omar Jawdat; Osama Almadhoun; Mamatha Pasnoor; April L McVey; Ahmad Abuzinadah; Laura Herbelin; Richard J Barohn; Mazen M Dimachkie
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

6.  A molecular analysis of the GAA gene and clinical spectrum in 38 patients with Pompe disease in Japan.

Authors:  Yasuyuki Fukuhara; Naoko Fuji; Narutoshi Yamazaki; Asami Hirakiyama; Tetsuharu Kamioka; Joo-Hyun Seo; Ryuichi Mashima; Motomichi Kosuga; Torayuki Okuyama
Journal:  Mol Genet Metab Rep       Date:  2017-10-31

7.  Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand.

Authors:  Lukana Ngiwsara; Duangrurdee Wattanasirichaigoon; Thipwimol Tim-Aroon; Kitiwan Rojnueangnit; Saisuda Noojaroen; Arthaporn Khongkraparn; Phannee Sawangareetrakul; James R Ketudat-Cairns; Ratana Charoenwattanasatien; Voraratt Champattanachai; Chulaluck Kuptanon; Suthipong Pangkanon; Jisnuson Svasti
Journal:  BMC Med Genet       Date:  2019-09-11       Impact factor: 2.103

8.  Enzyme activities of α-glucosidase in Japanese neonates with pseudodeficiency alleles.

Authors:  Ryuichi Mashima; Torayuki Okuyama
Journal:  Mol Genet Metab Rep       Date:  2017-07-07

9.  Investigation of newborns with abnormal results in a newborn screening program for four lysosomal storage diseases in Brazil.

Authors:  Heydy Bravo; Eurico Camargo Neto; Jaqueline Schulte; Jamile Pereira; Claudio Sampaio Filho; Fernanda Bittencourt; Fernanda Sebastião; Fernanda Bender; Ana Paula Scholz de Magalhães; Régis Guidobono; Franciele Barbosa Trapp; Kristiane Michelin-Tirelli; Carolina F M Souza; Diana Rojas Málaga; Gabriela Pasqualim; Ana Carolina Brusius-Facchin; Roberto Giugliani
Journal:  Mol Genet Metab Rep       Date:  2017-07-04

10.  Clinical and molecular characterization of Korean children with infantile and late-onset Pompe disease: 10 years of experience with enzyme replacement therapy at a single center.

Authors:  Min-Sun Kim; Ari Song; Minji Im; June Huh; I-Seok Kang; Jinyoung Song; Aram Yang; Jinsup Kim; Eun-Kyung Kwon; Eu-Jin Choi; Sun-Ju Han; Hyung-Doo Park; Sung Yoon Cho; Dong-Kyu Jin
Journal:  Korean J Pediatr       Date:  2018-10-04
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