Literature DB >> 18679824

Glycogen storage disease type I in Tunisia: an epidemiological analysis.

A Ben Chehida1, N Tebib, W Cherif, H Ben Turkia, S Abdelmoula, H Azzouz, M F Ben Dridi.   

Abstract

OBJECTIVE: Analysis of epidemiological data concerning GSD I in Tunisia. SUBJECTS AND METHODS: All the cases diagnosed as GSD I between 1992 and 2005 in a paediatric department recruiting all the metabolic diseases referred from the North of Tunisia were reviewed. Individual data (sex, socioeconomic and educational background, geographic origins, insurance coverage) were collected and pedigrees were reconstituted.
RESULTS: Twenty-two cases (9 boys and 13 girls from 20 homes) were identified. Fourteen belonged to 11 families originating from the North of Tunisia; ten of them are still alive. Both parents in 4 homes (21%) and one parent in 9 homes (47%) were illiterate. Most of the homes (60%) had a low income and 45% comprised at least 3 children. Only 7 homes (35%) had health insurance. Pedigrees indicated 44 infant deaths and at least 10 other cases fulfilling the clinical features of GSD I but not diagnosed.
CONCLUSION: The paediatric prevalence of GSD I in the North of Tunisia can be estimated to 7.93 cases per one million inhabitants and its incidence to 1/100,000 births. However, it is likely to be more frequent because of underreporting or underdiagnosis leading to precocious deaths.

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Year:  2008        PMID: 18679824     DOI: 10.1007/s10545-008-0707-2

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  14 in total

Review 1.  How many forms of glycogen storage disease type I?

Authors:  M Veiga-da-Cunha; I Gerin; E Van Schaftingen
Journal:  Eur J Pediatr       Date:  2000-05       Impact factor: 3.183

Review 2.  Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chart.

Authors:  J P Rake; A M ten Berge; G Visser; E Verlind; K E Niezen-Koning; C H Buys; G P Smit; H Scheffer
Journal:  Eur J Pediatr       Date:  2000-05       Impact factor: 3.183

3.  Type-1c glycogen storage disease is not caused by mutations in the glucose-6-phosphate transporter gene.

Authors:  B Lin; H Hiraiwa; C J Pan; R C Nordlie; J Y Chou
Journal:  Hum Genet       Date:  1999-11       Impact factor: 4.132

4.  [Biological and physiopathological aspects of hepatic glycogenoses].

Authors:  C Baussan; N Moatti; A Lemonnier
Journal:  Ann Gastroenterol Hepatol (Paris)       Date:  1988 Mar-Apr

5.  Biochemical diagnosis of type 1b glycogen storage disease.

Authors:  R A Hawkins; K R Kamath; S F Dorney; A Adams
Journal:  Aust Paediatr J       Date:  1984-08

6.  Glycogen storage disease type I: diagnosis and phenotype/genotype correlation.

Authors:  Dietrich Matern; Hans Hermann Seydewitz; Deeksha Bali; Christine Lang; Yuan-Tsong Chen
Journal:  Eur J Pediatr       Date:  2002-07-27       Impact factor: 3.183

Review 7.  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

Review 8.  Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.

Authors:  J I Wolfsdorf; I A Holm; D A Weinstein
Journal:  Endocrinol Metab Clin North Am       Date:  1999-12       Impact factor: 4.741

Review 9.  Glycogen storage disease in adults.

Authors:  G M Talente; R A Coleman; C Alter; L Baker; B I Brown; R A Cannon; Y T Chen; J F Crigler; P Ferreira; J C Haworth; G E Herman; R M Issenman; J P Keating; R Linde; T F Roe; B Senior; J I Wolfsdorf
Journal:  Ann Intern Med       Date:  1994-02-01       Impact factor: 25.391

10.  Type Ic, a novel glycogenosis. Underlying mechanism.

Authors:  R C Nordlie; K A Sukalski; J M Muñoz; J J Baldwin
Journal:  J Biol Chem       Date:  1983-08-25       Impact factor: 5.157

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