Page last updated: 2024-10-25

diazoxide and Tyrosinemias

diazoxide has been researched along with Tyrosinemias in 2 studies

Diazoxide: A benzothiadiazine derivative that is a peripheral vasodilator used for hypertensive emergencies. It lacks diuretic effect, apparently because it lacks a sulfonamide group.
diazoxide : A benzothiadiazine that is the S,S-dioxide of 2H-1,2,4-benzothiadiazine which is substituted at position 3 by a methyl group and at position 7 by chlorine. A peripheral vasodilator, it increases the concentration of glucose in the plasma and inhibits the secretion of insulin by the beta- cells of the pancreas. It is used orally in the management of intractable hypoglycaemia and intravenously in the management of hypertensive emergencies.

Tyrosinemias: A group of disorders which have in common elevations of tyrosine in the blood and urine secondary to an enzyme deficiency. Type I tyrosinemia features episodic weakness, self-mutilation, hepatic necrosis, renal tubular injury, and seizures and is caused by a deficiency of the enzyme fumarylacetoacetase. Type II tyrosinemia features INTELLECTUAL DISABILITY, painful corneal ulcers, and keratoses of the palms and plantar surfaces and is caused by a deficiency of the enzyme TYROSINE TRANSAMINASE. Type III tyrosinemia features INTELLECTUAL DISABILITY and is caused by a deficiency of the enzyme 4-HYDROXYPHENYLPYRUVATE DIOXYGENASE. (Menkes, Textbook of Child Neurology, 5th ed, pp42-3)

Research Excerpts

ExcerptRelevanceReference
"Hereditary tyrosinemia (HT1) is a rare metabolic disorder associated with accumulation of toxic metabolites of the tyrosine pathway due to a genetically mediated enzyme defect of fumarylacetoacetate hydrolase."5.62Neonatal hyperinsulinism in transient and classical forms of tyrosinemia. ( Gujral, J; Romero, CJ; Sethuram, S; Sperling, MA, 2021)
"Hereditary tyrosinemia (HT1) is a rare metabolic disorder associated with accumulation of toxic metabolites of the tyrosine pathway due to a genetically mediated enzyme defect of fumarylacetoacetate hydrolase."1.62Neonatal hyperinsulinism in transient and classical forms of tyrosinemia. ( Gujral, J; Romero, CJ; Sethuram, S; Sperling, MA, 2021)
"Treatment with diazoxide and chlorthiazide is highly effective, appears to be safe, and does not need to be continued lifelong."1.33Hyperinsulinism in tyrosinaemia type I. ( Baumann, U; Green, A; Kelly, DA; McKiernan, PJ; Preece, MA, 2005)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Sethuram, S1
Sperling, MA1
Gujral, J1
Romero, CJ1
Baumann, U1
Preece, MA1
Green, A1
Kelly, DA1
McKiernan, PJ1

Other Studies

2 other studies available for diazoxide and Tyrosinemias

ArticleYear
Neonatal hyperinsulinism in transient and classical forms of tyrosinemia.
    Orphanet journal of rare diseases, 2021, 04-28, Volume: 16, Issue:1

    Topics: Congenital Hyperinsulinism; Diazoxide; Humans; Hyperinsulinism; Infant; Infant, Newborn; Liver; Tyro

2021
Hyperinsulinism in tyrosinaemia type I.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:2

    Topics: Blood Glucose; C-Peptide; Chlorothiazide; Diazoxide; Diuretics; Humans; Hyperinsulinism; Hypoglycemi

2005