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Diseases » Mitochondrial diseases » Prevalence
 

Prevalence Statistics for Types of Mitochondrial diseases

Prevalence Statistics for Types of Mitochondrial diseases

The information below shows a list of types of Mitochondrial diseases, with information as to the prevalence of each of these types. Estimates of the people affected are calculated based on the available statistic.

Disease Prevalence Estimate US people estimate Statistic Used for Calculation
Leber's hereditary optic atrophy N/A N/A No information
Kearns-Sayre Syndrome N/A N/A rare
Progressive external ophthalmoplegia N/A N/A No information
Myoclonus epilepsy N/A N/A No information
MELAS N/A N/A No information
myoclonus epilepsy with ragged-red fibers (MERRF) N/A N/A No information
mitochondrial encephalopathies N/A N/A No information
Optic atrophy 1 N/A N/A No information
Pearson's anemia N/A N/A No information
Mitochondrial Parkinson's disease N/A N/A No information
Complex 5 mitochondrial respiratory chain deficiency N/A N/A No information
Complex 4 mitochondrial respiratory chain deficiency, benign infantile myopathy N/A N/A No information
Complex 4 mitochondrial respiratory chain deficiency, fatal infant myopathy type N/A N/A No information
Complex 1 mitochondrial respiratory chain deficiency N/A N/A No information
Complex 2 mitochondrial respiratory chain deficiency N/A N/A No information
Deafness, isolated, due to mitochondrial transmission N/A N/A No information
Friedreich's ataxia N/A N/A No information
Friedreich ataxia approx 1 in 40,000 or 0.00% or 6,800 people in USA 6,799 estimated 1 per 40,000 people are affected by Friedreich ataxia, Genetics Home Reference website
Diabetes insipidus, diabetes mellitus, optic atrophy, deafness, mitochondrial form N/A N/A No information
Friedreich ataxia -- congenital glaucoma N/A N/A No information
Beta ketothiolase deficiency approx 1 in 5,440,000 or 0.00% or 49 people in USA 49 50 - 60 cases of beta-ketothiolase deficiency have been reported worldwide, Genetics Home Reference website
Myopathy, Mitochonrdrial Progressive, with Congenital Cataract, Hearing Loss and Developmental Delay N/A N/A No information
Myopathy mitochondrial -- cataract N/A N/A No information
Mitochondrial encephalomyopathy -- aminoacidopathy N/A N/A No information
Mitochondrial myopathy -- lactic acidosis N/A N/A No information
MGA 4 N/A N/A No information
$2-methylglutaconic aciduria type 3$ approx 1 in 10,000 or 0.01% or 27,200 people in USA 27,199 1 per 10,000 newborns from Iraqi Jewish populations suffer from 2-methylglutaconic aciduria type 3, Genetics Home Reference website
$3-methylglutaconic aciduria, type 4$ N/A N/A No information
$3-methylglutaconic aciduria, type 1$ approx 1 in 13,600,000 or 0.00% or 20 people in USA 20 less than 20 cases of 2-methylglutaconic aciduria type 1 have been reported, Genetics Home Reference website
$3 alpha methylglutaconicaciduria, type 3$ N/A N/A No information
$3-methylglutaconic aciduria, type V$ N/A N/A No information
Barth Syndrome approx 1 in 400,000 or 0.00% or 680 people in USA 680 1 per 200,000 male infants suffer from 2-methylglutaconic aciduria type 2, Genetics Home Reference website
Pyruvate carboxylase deficiency approx 1 in 250,000 or 0.00% or 1,087 people in USA 1,087 estimated 1 per 250,000 births are affected by pyruvate carboxylase deficiency, Genetics Home Reference website
Pyruvate carboxylase deficiency, Group C N/A N/A No information
Pyruvate carboxylase deficiency, Group B N/A N/A No information
Pyruvate carboxylase deficiency, Group A N/A N/A No information
Pyruvate dehydrogenase deficiency N/A N/A No information
Mitochondrial trifunctional protein deficiency N/A N/A No information
Mitochondrial neurogastrointestinal encephalopathy syndrome N/A N/A No information
Mitochondrial DNA depletion syndrome N/A N/A No information
Mitochondrial diseases of nuclear origin N/A N/A No information
Wolfram Syndrome 2 N/A N/A No information
Wolfram Syndrome, Mitochondrial form N/A N/A No information
DIDMOAD Syndrome, Mitochondrial form N/A N/A No information
Leigh syndrome N/A N/A No information
Mitochondrial diseases, clinically indefinite N/A N/A No information
Leigh syndrome, Saguenay-Lac-St. Jean type N/A N/A No information
Leigh syndrome, French Canadian type N/A N/A No information
Maternally Inherited Leigh Syndrome N/A N/A No information

Types of Mitochondrial diseases

For more information about types of Mitochondrial diseases, refer to our section on types of Mitochondrial diseases.

About prevalence:

The medical term 'prevalence' of Mitochondrial diseases usually refers to the estimated population of people who are managing Mitochondrial diseases at any given time, whereas the annual diagnosis rate of new cases of Mitochondrial diseases is called the 'incidence'. For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.

 

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