Examples of 'dehydrogenase deficiency' in a sentence
Meaning of "dehydrogenase deficiency"
Dehydrogenase deficiency refers to a condition where there is a lack of a particular enzyme that is responsible for removing hydrogen atoms from a molecule
How to use "dehydrogenase deficiency" in a sentence
Basic
Advanced
dehydrogenase deficiency
Patients with succinic semialdehyde dehydrogenase deficiency.
This fatty aldehyde dehydrogenase deficiency is in fact a genetic disease.
Sodium oxybate is contraindicated in patients with succinic semialdehyde dehydrogenase deficiency.
If you have succinic semialdehyde dehydrogenase deficiency a rare metabolic disorder.
A ketogenic diet has been proposed for patients with pyruvate dehydrogenase deficiency.
People with pyruvate dehydrogenase deficiency usually have neurological problems as well.
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiency.
Pyruvate dehydrogenase deficiency can result from mutations in any of the enzymes or cofactors.
Succinic semialdehyde dehydrogenase deficiency.
Haemolytic reactions have been reported with ciprofloxacin in patients with glucose-6-phosphate dehydrogenase deficiency.
Succinic semialdehyde dehydrogenase deficiency is a disease that causes GHB to accumulate in the blood.
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency.
Medium-chain acyl-coenzyme A dehydrogenase deficiency can be caused by mutations in the ACADM gene.
At least 17 mutations in the DLD gene have been found to cause dihydrolipoamide dehydrogenase deficiency.
The main contraindications are glucose 6-phosphate dehydrogenase deficiency and simultaneous intake of zidovudine.
See also
Mutations in the ACADVL are associated with very long-chain acyl-coenzyme A dehydrogenase deficiency.
Patients with glucose-6-phosphate dehydrogenase deficiency risk haemolysis.
Exposure to naphthalene mothballs can cause acute hemolysis ( anemia ) in people with glucose-6-phosphate dehydrogenase deficiency.
Patients with glucose-6-phosphate dehydrogenase deficiency are at high risk for complications.
Haemolytic anaemia secondary to glucose-6-phosphate dehydrogenase deficiency.
Glucose-6-phosphate dehydrogenase deficiency ( G6PD deficiency ) is an inherited condition of the blood.
Long-chain hydroxyacyl-CoA dehydrogenase deficiency.
Observe caution in patients with blood disorders or glucose-6-phosphate dehydrogenase deficiency.
Each child with short-chain acyl-CoA dehydrogenase deficiency ( SCAD ) has a different experience.
If you or any member of your family have glucose-6-phosphate dehydrogenase deficiency a.
Patients with Glucose-6-phosphate dehydrogenase deficiency ( G6PD ) due to the risk of haemolytic anaemia.
Hemolytic anemia secondary to glucose-6-phosphate dehydrogenase deficiency.
Persons with glucose-6-phosphate dehydrogenase deficiency ( G6PD ) may develop hemolytic anemia from primaquine.
Patients with a family history of, or actual glucose-6-phosphate dehydrogenase deficiency are.
Priapism may also be associated with glucose-6-phosphate dehydrogenase deficiency which leads to decreased NADPH levels.
It must not be used in patients with the following conditions, glucose-6-phosphate dehydrogenase deficiency G6PD.
Long-chain acyl-CoA dehydrogenase deficiency.
Over 400 million people have an inherited condition called glucose-6-phosphate dehydrogenase deficiency.
Glucose 6-phosphate dehydrogenase deficiency.
Mallouh AA, Abu-Osba YK ; Bacterial infections in children with glucose-6-phosphate dehydrogenase deficiency.
Patients with G-6-phosphate dehydrogenase deficiency.
A deficiency is associated with 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Not all children with long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency ( ICHAD ) show signs of the condition.
More than 30 ACADM gene mutations that cause medium-chain acyl-coenzyme A dehydrogenase deficiency have been identified.
Patients with glucose-6-phosphate dehydrogenase deficiency.
Patients with G-6 - phosphate dehydrogenase deficiency.
You'll also be interested in:
Examples of using Deficiency
Show more
It is caused by a deficiency of thyroid hormone in newborn infants
Final inspection of site and deficiency work
Manganese deficiency appears similar to iron deficiency
Examples of using Dehydrogenase
Show more
Increased lactate dehydrogenase level in your blood
Retinoid compounds are eliminated via alcohol dehydrogenase
An increase in lactate dehydrogenase is common but nonspecific
