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Hyperoxaluria type I: therapeutic effects of pyridoxine hydrochloride and inheritance patterns of the disease in a family
- Source :
- The Kurume medical journal. 35(3)
- Publication Year :
- 1988
-
Abstract
- The cases of two patients with primary hyperoxaluria type I, aged five years and two years, born to consanguineous parents are described. These patients have been treated with oral pyridoxine hydrochloride at a dose of 200mg/24 hr without evidence that this regimen has decreased urinary oxalate excretion. Studies of oxalate excretion in the family members yielded results consistent with either autosomal dominant inheritance, with variable expressivity, or with autosomal recessive character.
- Subjects :
- Male
medicine.medical_specialty
Urinary system
Physiology
Oxalate
Excretion
chemistry.chemical_compound
Internal medicine
Primary Hyperoxaluria Type I
Medicine
Inheritance Patterns
Humans
Child
Pyridoxine Hydrochloride
Hyperoxaluria
business.industry
Therapeutic effect
Pyridoxine
General Medicine
Pedigree
Regimen
Endocrinology
chemistry
Child, Preschool
Hyperoxaluria, Primary
Female
business
Subjects
Details
- ISSN :
- 00235679
- Volume :
- 35
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- The Kurume medical journal
- Accession number :
- edsair.doi.dedup.....d109397b10646af659d30eac518c6c44