Page last updated: 2024-10-27

furosemide and Hypophosphatasia

furosemide has been researched along with Hypophosphatasia in 1 studies

Furosemide: A benzoic-sulfonamide-furan. It is a diuretic with fast onset and short duration that is used for EDEMA and chronic RENAL INSUFFICIENCY.
furosemide : A chlorobenzoic acid that is 4-chlorobenzoic acid substituted by a (furan-2-ylmethyl)amino and a sulfamoyl group at position 2 and 5 respectively. It is a diuretic used in the treatment of congestive heart failure.

Hypophosphatasia: A genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia. Clinical manifestations include severe skeletal defects resembling vitamin D-resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. (From Dorland, 27th ed)

Research Excerpts

ExcerptRelevanceReference
"Hypophosphatasia is a rare inherited disorder of bone and mineral metabolism caused by a number of loss-of-function mutations in the ALPL gene."5.43Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene. ( Bircan, İ; Çelmeli, G; Güzel Nur, B; Manguoğlu, E; Mıhçı, E; Soyucen, E, 2016)
"Hypophosphatasia is a rare inherited disorder of bone and mineral metabolism caused by a number of loss-of-function mutations in the ALPL gene."1.43Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene. ( Bircan, İ; Çelmeli, G; Güzel Nur, B; Manguoğlu, E; Mıhçı, E; Soyucen, E, 2016)

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
Güzel Nur, B1
Çelmeli, G1
Manguoğlu, E1
Soyucen, E1
Bircan, İ1
Mıhçı, E1

Other Studies

1 other study available for furosemide and Hypophosphatasia

ArticleYear
Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene.
    Journal of clinical research in pediatric endocrinology, 2016, Sep-01, Volume: 8, Issue:3

    Topics: Alkaline Phosphatase; Calcitonin; Diuretics; Female; Furosemide; Homozygote; Humans; Hypophosphatasi

2016