Literature DB >> 1057811

Incidence of glycogen storage disease in the German Federal Republic.

J Schaub, P Bayerl.   

Abstract

100 cases of GSD were traced in the GFR. The overall incidence is 1:113000 in proportion to live births. Type I occurs most frequently with 30%, followed by Type II and Type VI with 20% each. Type III is extremely rate in the GFR. 5 cases were classified as glycogenosis with the Fanconi syndrome. With the exception of Type III the type distribution in the GFR was similar to that found in 316 cases in a diagnostic center in Belgium.

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Year:  1975        PMID： 1057811     DOI： 10.1007/bf00445157

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN： 0044-2917


  15 in total

1.  [GLYCOGENOSIS OF THE LIVER WITH AMINOACIDURIA AND GLYCOSURIA. CLINICAL AND BIOCHEMICAL STUDIES].

Authors:  H W ROTTHAUWE; H FICHSEL; H W HELDT; E KIRSTEN; M REIM; E SCHMIDT; F W SCHMIDT; W WESEMANN
Journal:  Klin Wochenschr       Date:  1963-08-15

2.  GLYCOGEN STORAGE DISEASE. BIOCHEMICAL AND CLINICAL DATA IN SIXTEEN CASES.

Authors:  F HUIJING
Journal:  Am J Med       Date:  1965-04       Impact factor: 4.965

3.  GLYCOGEN STORAGE DISEASE IN SWEDEN.

Authors:  P A OCKERMAN
Journal:  Acta Paediatr Scand       Date:  1965

4.  [Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease].

Authors:  G FANCONI; H BICKEL
Journal:  Helv Paediatr Acta       Date:  1949-11

5.  The estimation of glycogen with the anthrone reagent.

Authors:  S SEIFTER; S DAYTON
Journal:  Arch Biochem       Date:  1950-01

6.  Glycogen storage diseases.

Authors:  F Van Hoof; L Hue; T De Barsy; P Jacquemin; P Devos; H G Hers
Journal:  Biochimie       Date:  1972       Impact factor: 4.079

7.  Incidence of glycogen storage disease in Sweden.

Authors:  P A Ockerman
Journal:  Acta Paediatr Scand       Date:  1972-09

8.  The subgroups of type 3 glycogenosis.

Authors:  F Van Hoof; H G Hers
Journal:  Eur J Biochem       Date:  1967-10

9.  [Glycogenosis of the liver with galactose utilization disorder and a severe Fanconi syndrome].

Authors:  F Lampert; H Mayer
Journal:  Z Kinderheilkd       Date:  1967

10.  [Debré-De Toni-Fanconi syndrome with glycogenosis of the liver].

Authors:  B Bauer
Journal:  Klin Wochenschr       Date:  1968-03-15
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  2 in total

1.  Ethanolaminosis. A newly recognized, generalized storage disease with cardiomegaly, cerebral dysfunction and early death.

Authors:  K W Vietor; B Havsteen; D Harms; H Busse; K Heyne
Journal:  Eur J Pediatr       Date:  1977-08-23       Impact factor: 3.183

2.  Chronic inflammatory bowel disease in glycogen storage disease type 1B.

Authors:  I R Sanderson; W M Bisset; P J Milla; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982
  2 in total

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