Lactate dehydrogenase deficiency

Common Name(s)

Lactate dehydrogenase deficiency

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Lactate dehydrogenase deficiency" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Lactate dehydrogenase deficiency" returned 7 free, full-text research articles on human participants. First 3 results:

Hereditary deficiency of lactate dehydrogenase H-subunit.
 

Author(s): H Wakabayashi, M Tsuchiya, K Yoshino, K Kaku, H Shigei

Journal: Intern. Med.. 1996 Jul;35(7):550-4.

 

We report herein the fifth family of hereditary deficiency of lactate dehydrogenase (LDH) H-subunit with an autosomal recessive inheritance including two cases of complete deficiency. Their LDH activities were low both in the serum and in the red blood cells (RBC). Electrophoretic ...

Last Updated: 9 Jan 1997

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Characterization of the oxidative metabolism in lactate dehydrogenase A deficiency.
 

Author(s): H Miyajima, Y Takahashi, E Kaneko

Journal: Intern. Med.. 1995 Jun;34(6):502-6.

 

Recurrent rhabdomyolysis due to decreased glycolysis occurred during strenuous exercise in patients with lactate dehydrogenase A subunit (LDH-A) deficiency. We report the features of oxidative metabolism of four patients from two families in whom the severity of the disease differed. ...

Last Updated: 26 Oct 1995

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Genetic analysis of a family of lactate dehydrogenase A subunit deficiency.
 

Author(s): Y Takahashi, H Miyajima, E Kaneko

Journal: Intern. Med.. 1995 May;34(5):326-9.

 

Lactate dehydrogenase A subunit (LDH-A) deficiency is an inherited metabolic myopathy of glycolysis. The severity of this disease varies from case to case. We reported non-consanguineous male sibling cases who had severe muscle pain and rhabdomyolysis during anaerobic exercise. Genetic ...

Last Updated: 26 Sep 1995

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Reviews from the PubMed Database

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The terms "Lactate dehydrogenase deficiency" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.