Biochemical characteristics and increased tetraglucoside excretion in patients with phosphorylase kinase deficiency
- PMID: 16151901
- DOI: 10.1007/s10545-005-0095-9
Biochemical characteristics and increased tetraglucoside excretion in patients with phosphorylase kinase deficiency
Abstract
Patients with glycogen storage disease type IXa present with infantile hepatomegaly and a specific growth pattern, and variable biochemical alterations in blood. We studied the clinical and biochemical characteristics including the urinary oligosaccharide excretion of seven unrelated children. The urinary tetraglucoside excretion was increased in four children, three of whom had persistently high cholesterol and triglyceride concentrations. We propose screening for urine tetraglucoside excretion and the measurement of serum cholesterol in patients with growth delay and/or hepatomegaly to assess a possible glycogenosis.
Similar articles
-
[Glycogenosis due to a defect of liver phosphorylase-kinase (glycogenosis type IX). A clinical, biochemical, and electron-microscopy study].Acta Med Iugosl. 1978;32(1):75-91. Acta Med Iugosl. 1978. PMID: 274067 Croatian. No abstract available.
-
Dextrothyroxine treatment of phosphorylase-kinase deficiency glycogenosis in four boys.Helv Paediatr Acta. 1978 Nov;33(4-5):435-41. Helv Paediatr Acta. 1978. PMID: 280544
-
Infantile hypertrophic cardiomyopathy of glycogenosis type IX: isolated cardiac phosphorylase kinase deficiency.Pediatr Cardiol. 1999 Jul-Aug;20(4):304-7. doi: 10.1007/s002469900471. Pediatr Cardiol. 1999. PMID: 10368461
-
GLYCOGEN STORAGE DISEASE.Adv Metab Disord. 1964;13:1-44. doi: 10.1016/b978-1-4831-6748-0.50006-9. Adv Metab Disord. 1964. PMID: 14171618 Review. No abstract available.
-
Fatal infantile hypertrophic cardiomyopathy secondary to deficiency of heart specific phosphorylase b kinase.Virchows Arch A Pathol Anat Histopathol. 1993;423(4):303-7. doi: 10.1007/BF01606895. Virchows Arch A Pathol Anat Histopathol. 1993. PMID: 8236826 Review.
Cited by
-
Biomarkers in Glycogen Storage Diseases: An Update.Int J Mol Sci. 2021 Apr 22;22(9):4381. doi: 10.3390/ijms22094381. Int J Mol Sci. 2021. PMID: 33922238 Free PMC article. Review.
-
Clinical, Biochemical, and Genetic Characterization of Glycogen Storage Type IX in a Child with Asymptomatic Hepatomegaly.Pediatr Gastroenterol Hepatol Nutr. 2015 Jun;18(2):138-43. doi: 10.5223/pghn.2015.18.2.138. Epub 2015 Jun 29. Pediatr Gastroenterol Hepatol Nutr. 2015. PMID: 26157701 Free PMC article.
-
Urine glucose tetrasaccharide: A good biomarker for glycogenoses type II and III? A study of the French cohort.Mol Genet Metab Rep. 2020 May 1;23:100583. doi: 10.1016/j.ymgmr.2020.100583. eCollection 2020 Jun. Mol Genet Metab Rep. 2020. PMID: 32382504 Free PMC article. No abstract available.
-
Clinical and Molecular Variability in Patients with PHKA2 Variants and Liver Phosphorylase b Kinase Deficiency.JIMD Rep. 2017;37:63-72. doi: 10.1007/8904_2017_8. Epub 2017 Mar 12. JIMD Rep. 2017. PMID: 28283841 Free PMC article.
-
Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene.Mol Genet Metab. 2014 Mar;111(3):309-313. doi: 10.1016/j.ymgme.2013.12.008. Epub 2013 Dec 19. Mol Genet Metab. 2014. PMID: 24389071 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources