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Literature DB >> 7073302

Oxalosis in infancy.

M C Morris, T L Chambers, P W Evans, P N Malleson, J R Pincott, G A Rose.

Abstract

We describe 3 infants with nephrocalcinosis and terminal renal failure. In all 3 there was widespread oxalate deposition: biochemical evidence of primary hyperoxaluria was sought but the presence of severe renal failure and the lack of established normal values for urinary and plasma oxalate and glycollate in infants made this diagnosis difficult to establish.

Entities: Chemical Disease Species

Mesh：

Substances：
Calcium Oxalate

Year: 1982 PMID： 7073302 PMCID： PMC1627612 DOI： 10.1136/adc.57.3.224

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

14 in total

1. Oxalosis; possible inborn error of metabolism with nephrolithiasis and nephrocalcinosis due to calcium oxalate as the predominating features.

Authors: L Y CHOU; W L DONOHUE
Journal: Pediatrics Date: 1952-12 Impact factor: 7.124

2. An unusual case of calcium oxalate deposits in the kidney of a young infant.

Authors: M MULLOY
Journal: J Pediatr Date: 1951-08 Impact factor: 4.406

Review 3. Oxalic acid and the hyperoxaluric syndromes.

Authors: H E Williams
Journal: Kidney Int Date: 1978-05 Impact factor: 10.612

4. The variation of urinary oxalate excretion with age.

Authors: D A Gibbs; R W Watts
Journal: J Lab Clin Med Date: 1969-06

Review 5. Histopathological occurrence and characterisation of calcium oxalate: a review.

Authors: A J Chaplin
Journal: J Clin Pathol Date: 1977-09 Impact factor: 3.411

6. Ophthalmic manifestations of primary oxalosis.

Authors: A R Fielder; A Garner; T L Chambers
Journal: Br J Ophthalmol Date: 1980-10 Impact factor: 4.638

7. Studies on some possible biochemical treatments of primary hyperoxaluria.

Authors: R W Watts; R A Chalmers; D A Gibbs; A M Lawson; P Purkiss; E Spellacy
Journal: Q J Med Date: 1979-04

8. "Flecked retina" --an association with primary hyperoxaluria.

Authors: R P Gottlieb; J A Ritter
Journal: J Pediatr Date: 1977-06 Impact factor: 4.406

9. Primary oxalosis: clinical and biochemical response to high-dose pyridoxine therapy.

Authors: E J Will; O L Bijvoet
Journal: Metabolism Date: 1979-05 Impact factor: 8.694

10. Plasma level and renal clearance of oxalate in normal subjects and in patients with primary hyperoxaluria or chronic renal failure or both.

Authors: A R Constable; A M Joekes; G P Kasidas; P O'Regan; G A Rose
Journal: Clin Sci (Lond) Date: 1979-04 Impact factor: 6.124

6 in total

Oxalosis in infancy.

1. Oxalosis; possible inborn error of metabolism with nephrolithiasis and nephrocalcinosis due to calcium oxalate as the predominating features.

2. An unusual case of calcium oxalate deposits in the kidney of a young infant.

Review 3. Oxalic acid and the hyperoxaluric syndromes.

4. The variation of urinary oxalate excretion with age.

Review 5. Histopathological occurrence and characterisation of calcium oxalate: a review.

6. Ophthalmic manifestations of primary oxalosis.

7. Studies on some possible biochemical treatments of primary hyperoxaluria.

8. "Flecked retina" --an association with primary hyperoxaluria.

9. Primary oxalosis: clinical and biochemical response to high-dose pyridoxine therapy.

10. Plasma level and renal clearance of oxalate in normal subjects and in patients with primary hyperoxaluria or chronic renal failure or both.

1. Clinical quiz. Primary hyperoxaluria (PH) type 1.

2. Urinary oxalate and glycolate excretion in healthy infants and children.

3. [Type I oxalosis in childhood--studies within the scope of terminal renal failure in the child].

4. New aspects of infantile oxalosis.

Review 5. Bone disease of primary hyperoxaluria in infancy.

6. Renal failure due to 2,8-dihydroxyadenine urolithiasis.