Literature DB >> 8362811

Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency.

S A Sanjad1, R E Kaddoura, H M Nazer, M Akhtar, N A Sakati.   

Abstract

OBJECTIVE: To describe two patients with Fanconi's nephropathy secondary to glycogen storage disease and speculate on the possible etiology.
DESIGN: Convenience sample.
SETTING: Tertiary care, referral center. PATIENTS: Two related children referred for failure to thrive, rickets, and hepatomegaly. INTERVENTION: Dietary and therapeutic measures for rickets and renal tubular acidosis. MEASUREMENTS AND
RESULTS: The main laboratory findings were fasting hypoglycemia and massive glucosuria, with evidence of multiple renal tubular dysfunction characteristic of the Fanconi syndrome. Liver and kidney biopsy specimens were consistent with glycogen storage disease. Enzymatic assay of liver homogenates revealed marked deficiency of phosphorylase b kinase in one patient and absent activity in the other.
CONCLUSION: Phosphorylase b kinase deficiency may be causally related to hepatorenal glycogenosis with the Fanconi syndrome. More patients with this syndrome need to be studied before a definitive causal role is implicated.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8362811     DOI: 10.1001/archpedi.1993.02160330047016

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  5 in total

Review 1.  Inherited epithelial transporter disorders--an overview.

Authors:  M J Bergeron; A Simonin; M Bürzle; M A Hediger
Journal:  J Inherit Metab Dis       Date:  2008-04-14       Impact factor: 4.982

2.  Fanconi-Bickel syndrome as an example of marked allelic heterogeneity.

Authors:  Mohammad Al-Haggar
Journal:  World J Nephrol       Date:  2012-06-06

3.  Catch-up growth in Fanconi-Bickel syndrome with uncooked cornstarch.

Authors:  P J Lee; W G Van't Hoff; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

4.  Glomerular and tubular function in glycogen storage disease.

Authors:  P J Lee; R N Dalton; V Shah; P C Hindmarsh; J V Leonard
Journal:  Pediatr Nephrol       Date:  1995-12       Impact factor: 3.714

5.  No mutation in the SLC2A2 ( GLUT2) gene in a Turkish infant with Fanconi-Bickel syndrome.

Authors:  Esra Arun Ozer; Nejat Aksu; Erkan Uclar; Hakan Erdogan; Ali Rahmi Bakiler; Masahiko Tsuda; Emiko Kitasawa; Mahmut Coker; Erdener Ozer
Journal:  Pediatr Nephrol       Date:  2003-03-11       Impact factor: 3.714

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.