Literature DB >> 668712

Hyperglycinuria with nephrolithiasis.

V Oberiter, Z Puretić, V Fabecić-Sabadi.   

Abstract

The case of a seven and a half-year-old girl with hyperglycinuria, oxalate nephrolithiasis, and a normal plasma amino acid pattern is presented. Hyperglycinuria amounted to 400 mg of glycine in 24 h urine and the stone was composed of calcium oxalate dihydrate. The metabolic relationship between glycine and oxalate is discussed. It is possible that the association of nephrolithiasis and hyperglycinuria was coincidental, although the case of familial hyperglycinuria with nephrolithiasis reported by De Vries and collaborators and our case suggest the possibility of a relationship between the aforesaid compounds in vivo.

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Year:  1978        PMID: 668712     DOI: 10.1007/BF00493544

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


  18 in total

1.  THE RENAL CLEARANCE OF OXALIC ACID IN NORMAL SUBJECTS AND IN PATIENTS WITH PRIMARY HYPEROXALURIA.

Authors:  P M ZAREMBSKI; A HODGKINSON
Journal:  Invest Urol       Date:  1963-07

Review 2.  VITAMIN B6 AND OXALATE METABOLISM.

Authors:  S N GERSHOFF
Journal:  Vitam Horm       Date:  1964       Impact factor: 3.421

3.  Glycinuria, a hereditary disorder associated with nephrolithiasis.

Authors:  A DE VRIES; S KOCHWA; J LAZEBNIK; M FRANK; M DJALDETTI
Journal:  Am J Med       Date:  1957-09       Impact factor: 4.965

4.  The aetiology of primary hyperoxaluria.

Authors:  H E ARCHER; A E DORMER; E F SCOWEN; R W WATTS
Journal:  Br Med J       Date:  1958-01-25

5.  Identification and analysis of multiple glycine transport systems in isolated mammalian renal tubules.

Authors:  R E Hillman; I Albrecht; L E Rosenberg
Journal:  J Biol Chem       Date:  1968-11-10       Impact factor: 5.157

6.  Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids.

Authors:  M L Greene; P S Lietman; L E Rosenberg; J E Seegmiller
Journal:  Am J Med       Date:  1973-02       Impact factor: 4.965

Review 7.  Human genetics of membrane transport with emphasis on amino acids.

Authors:  C R Scriver; P Hechtman
Journal:  Adv Hum Genet       Date:  1970

8.  [Diagnosis and course of oxalosis. Histological and biochemical studies].

Authors:  K Beyreiss; U Willnow; R Schippan
Journal:  Kinderarztl Prax       Date:  1971-11

9.  Endogenous renal clearance rates of free amino acids in pre-pubertal children. (Employing an accelerated procedure for elution chromatography of basic amino acids on ion exchange resin).

Authors:  C R Scriver; E Davies
Journal:  Pediatrics       Date:  1965-10       Impact factor: 7.124

10.  The inhibition of oxalate biosynthesis in isolated perfused rat liver by DL-phenyllactate and n-heptanoate.

Authors:  L L Liao; K E Richardson
Journal:  Arch Biochem Biophys       Date:  1973-01       Impact factor: 4.013

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