Literature DB >> 6749505

Growth and endocrine changes in the hepatic glycogenoses.

D B Dunger, A T Holder, J V Leonard, J Okae, M A Preece.   

Abstract

The biochemical and endocrine responses of 13 patients with hepatic glycogen storage disease (HGSD) (type I-six patients, type Ib-two, type III-three, type IX-two patients) to an oral glucose load have been investigated. Longitudinal growth data was available in all patients. The height velocity standard deviation score (HVSDS) was positively correlated with the plasma somatomedin and inversely correlated with the glucose-insulin ratio, plasma cortisol and plasma growth hormone concentrations. There was no correlation between plasma glucagon and HVSDS with treatment was accompanied by a rise in plasma somatomedin and a fall in growth hormone and cortisol. In two patients the glucose-insulin ratio decreased. Growth retardation in HGSD can be explained as part of the adaptation to the inability to maintain normal glucose homeostasis.

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Year:  1982        PMID: 6749505     DOI: 10.1007/BF00441207

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  21 in total

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Journal:  J Biol Chem       Date:  1973-03-25       Impact factor: 5.157

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Journal:  J Clin Endocrinol Metab       Date:  1972-08       Impact factor: 5.958

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Journal:  Lancet       Date:  1978-01-14       Impact factor: 79.321

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Journal:  Endocrinology       Date:  1976-05       Impact factor: 4.736

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Journal:  J Clin Endocrinol Metab       Date:  1977-05       Impact factor: 5.958

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  10 in total

1.  The natural history of liver glycogenosis due to phosphorylase kinase deficiency: a longitudinal study of 41 patients.

Authors:  P J Willems; W J Gerver; R Berger; J Fernandes
Journal:  Eur J Pediatr       Date:  1990-01       Impact factor: 3.183

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Authors:  J E Collins; K Bartlett; J V Leonard; A Aynsley-Green
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Uncooked cornstarch treatment for hepatic phosphorylase kinase deficiency.

Authors:  A Nakai; Y Shigematsu; T Takano; Y Kikawa; M Sudo
Journal:  Eur J Pediatr       Date:  1994-08       Impact factor: 3.183

4.  Pathogenesis of growth failure and partial reversal with gene therapy in murine and canine Glycogen Storage Disease type Ia.

Authors:  Elizabeth Drake Brooks; Dianne Little; Ramamani Arumugam; Baodong Sun; Sarah Curtis; Amanda Demaster; Michael Maranzano; Mark W Jackson; Priya Kishnani; Michael S Freemark; Dwight D Koeberl
Journal:  Mol Genet Metab       Date:  2013-04-06       Impact factor: 4.797

5.  Hypogonadotropic Hypogonadism in Males with Glycogen Storage Disease Type 1.

Authors:  Evelyn M Wong; Anna Lehman; Philip Acott; Jane Gillis; Daniel L Metzger; Sandra Sirrs
Journal:  JIMD Rep       Date:  2017-02-04

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Authors:  P J Lee; J S Patel; M Fewtrell; J V Leonard; N J Bishop
Journal:  Eur J Pediatr       Date:  1995-06       Impact factor: 3.183

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Authors:  D B Dunger; J V Leonard; M A Preece
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8.  Glycogen storage disease presenting as Cushing syndrome.

Authors:  Margaret A Stefater; Joseph I Wolfsdorf; Nina S Ma; Joseph A Majzoub
Journal:  JIMD Rep       Date:  2019-04-03

9.  Bone mineral density in children, adolescents and adults with glycogen storage disease type Ia: a cross-sectional and longitudinal study.

Authors:  J P Rake; G Visser; D Huismans; S Huitema; E van der Veer; D A Piers; G P A Smit
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.750

10.  Imbalanced cortisol concentrations in glycogen storage disease type I: evidence for a possible link between endocrine regulation and metabolic derangement.

Authors:  Alessandro Rossi; Chiara Simeoli; Mariacarolina Salerno; Rosario Ferrigno; Roberto Della Casa; Annamaria Colao; Pietro Strisciuglio; Giancarlo Parenti; Rosario Pivonello; Daniela Melis
Journal:  Orphanet J Rare Dis       Date:  2020-04-19       Impact factor: 4.123

  10 in total

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