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pyridoxine and Familial Hypophosphatemic Rickets

pyridoxine has been researched along with Familial Hypophosphatemic Rickets in 1 studies

4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol: structure in first source
vitamin B6 : Any member of the group of pyridines that exhibit biological activity against vitamin B6 deficiency. Vitamin B6 deficiency is associated with microcytic anemia, electroencephalographic abnormalities, dermatitis with cheilosis (scaling on the lips and cracks at the corners of the mouth) and glossitis (swollen tongue), depression and confusion, and weakened immune function. Vitamin B6 consists of the vitamers pyridoxine, pyridoxal, and pyridoxamine and their respective 5'-phosphate esters (and includes their corresponding ionized and salt forms).

Familial Hypophosphatemic Rickets: A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.

Research Excerpts

ExcerptRelevanceReference
"Refractory rickets with Wilson's disease has been infrequently reported in literature."1.37Neurological Wilson's disease with refractory rickets. ( Aneja, S; Kaur, S; Krishnamurthy, S; Maheshwari, A; Patra, S; Seth, A, 2011)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kaur, S1
Maheshwari, A1
Aneja, S1
Patra, S1
Krishnamurthy, S1
Seth, A1

Other Studies

1 other study available for pyridoxine and Familial Hypophosphatemic Rickets

ArticleYear
Neurological Wilson's disease with refractory rickets.
    Journal of pediatric endocrinology & metabolism : JPEM, 2011, Volume: 24, Issue:3-4

    Topics: Adolescent; Calcitriol; Consanguinity; Drug Therapy, Combination; Familial Hypophosphatemic Rickets;

2011