Mitochondrial disease is a group of disorders caused by mitochondrial dysfunction. Mitochondria are the organelles that generate energy for the cell and...
33 KB (3,499 words) - 10:06, 30 May 2024
Mitochondrial DNA depletion syndrome (MDS or MDDS), or Alper's disease, is any of a group of autosomal recessive disorders that cause a significant drop...
23 KB (2,562 words) - 19:54, 23 August 2024
Mitochondrion (redirect from Mitochondrial membrane)
been implicated in several human disorders and conditions, such as mitochondrial diseases, cardiac dysfunction, heart failure and autism. The number of mitochondria...
166 KB (18,358 words) - 23:39, 24 August 2024
sustaining life. The mitochondrial diseases are genetic disorders carried in mitochondrial DNA, or nuclear DNA coding for mitochondrial components. Slight...
38 KB (4,014 words) - 00:17, 9 August 2024
Mitochondrial myopathies are types of myopathies associated with mitochondrial disease. Adenosine triphosphate (ATP), the chemical used to provide energy...
40 KB (3,236 words) - 05:10, 5 August 2024
haplogroup Human mitochondrial genetics Mitochondrial disease Mitochondrial DNA (journal) Mitochondrial Eve Mitochondrial rCRS Paternal mtDNA transmission Single...
95 KB (10,004 words) - 19:49, 14 August 2024
MELAS syndrome (redirect from Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like syndrome)
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the family of mitochondrial diseases, which also include MIDD...
16 KB (1,759 words) - 06:36, 2 May 2024
Green ribbon (section Mitochondrial disease)
variety of symbolic meanings. Mitochondrial disease awareness is represented by a green ribbon. Mitochondrial disease (mito) is a debilitating genetic...
18 KB (1,667 words) - 22:18, 21 June 2024
Mougey EB, O'Brien TW (March 2003). "Mitochondrial ribosomal proteins: candidate genes for mitochondrial disease". Genetics in Medicine. 6 (2): 73–80...
11 KB (1,081 words) - 15:58, 14 December 2023
or ameliorate disease. MRT originated as a special form of in vitro fertilisation in which some or all of the future baby's mitochondrial DNA (mtDNA) comes...
41 KB (4,636 words) - 11:47, 17 August 2024
Leigh syndrome (redirect from Leigh’s Disease)
Mutations in mitochondrial DNA (mtDNA) and over 30 genes in nuclear DNA (gene SURF1 and some COX assembly factors) have been implicated in Leigh disease. Disorders...
28 KB (3,197 words) - 19:54, 23 August 2024
encephalopathy, also called mad cow disease. The greatest risk factor for neurodegenerative diseases is aging. Mitochondrial DNA mutations as well as oxidative...
63 KB (6,937 words) - 02:47, 25 August 2024
Metabolic disorder (redirect from Metabolic disease)
error of metabolism Mitochondrial diseases Phosphorus metabolism disorders Porphyrias Proteostasis deficiencies Metabolic skin diseases Wasting syndrome...
10 KB (771 words) - 03:15, 8 August 2024
genome (mitochondrial DNA or plastid DNA) within a cell or individual. It is an important factor in considering the severity of mitochondrial diseases. Because...
18 KB (2,268 words) - 12:58, 3 December 2023
Environmental disease Host–pathogen interaction Lists of diseases Mitochondrial disease Philosophy of medicine Plant pathology Rare disease, a disease that affects...
62 KB (7,102 words) - 12:13, 8 August 2024
Leber's hereditary optic neuropathy (redirect from Leber's disease)
mutations in the mitochondrial (not nuclear) genome, and only the egg contributes mitochondria to the embryo. Men cannot pass on the disease to their offspring...
41 KB (4,613 words) - 19:54, 23 August 2024
Dysautonomia (redirect from Dysautonomia (does not have to be familial) (Autonomic Nervous System Diseases))
pressure support mode in a patient with autonomic dysfunction and mitochondrial disease". Journal of Clinical Sleep Medicine. 17 (4): 853–857. doi:10.5664/jcsm...
28 KB (2,665 words) - 06:16, 10 July 2024
MERRF syndrome (category Mitochondrial diseases)
MERRF syndrome (or myoclonic epilepsy with ragged red fibers) is a mitochondrial disease. It is extremely rare, and has varying degrees of expressivity owing...
18 KB (1,929 words) - 14:57, 22 April 2024
congenital disorders List of ICD-9 codes 740-759: Congenital anomalies Mitochondrial disease Eze KC, Akhigbe AO, Awosanya GO (September 2007). "Fibular hemimelia:...
8 KB (725 words) - 07:21, 15 July 2024
ALS (redirect from Lou Gehrigs disease)
Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND) or Lou Gehrig's disease in the United States, is a rare, terminal neurodegenerative...
130 KB (14,040 words) - 08:10, 18 August 2024
Mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE) is a rare autosomal recessive mitochondrial disease. It has been previously referred...
9 KB (800 words) - 20:06, 6 December 2023
Mitochondrial cytopathy (generic term) Mitochondrial diseases of nuclear origin Mitochondrial diseases, clinically undefinite Mitochondrial disease Mitochondrial...
28 KB (2,469 words) - 04:35, 13 June 2024
Pearson syndrome (category Mitochondrial diseases)
Pearson syndrome is a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Other clinical features are failure...
12 KB (1,198 words) - 18:37, 26 January 2024
Dementia with Lewy bodies (redirect from Diffuse Lewy body disease)
automatic bodily functions. Memory loss is not always an early symptom. The disease worsens over time and is usually diagnosed when cognitive impairment interferes...
136 KB (14,528 words) - 18:35, 30 July 2024
Chorea (redirect from Chorea (disease))
iron accumulation disorders, Wilson's disease, benign hereditary chorea, Friedreich's ataxia, mitochondrial disease and Rett syndrome. The most common acquired...
9 KB (727 words) - 11:08, 12 July 2024
Friedreich's ataxia (category Mitochondrial diseases)
metabolic dysfunction in Friedreich ataxia, an autosomal recessive mitochondrial disease". Neuronal Signaling. 2 (4): NS20180060. doi:10.1042/NS20180060...
46 KB (4,873 words) - 19:53, 23 August 2024
Restless legs syndrome (redirect from Ekbom Disease)
also known as restless leg syndrome (RLS), also known as Willis–Ekbom disease (WED), is a neurological disorder, usually chronic, that causes an overwhelming...
79 KB (8,316 words) - 13:15, 16 August 2024
Creatine (section Mitochondrial diseases)
immobilization. Creatine's impact on mitochondrial function has led to research on its efficacy and safety for slowing Parkinson's disease. As of 2014, the evidence...
64 KB (6,854 words) - 03:24, 17 August 2024
Chronic progressive external ophthalmoplegia (category Mitochondrial diseases)
feature of mitochondrial disease, in which case the term CPEO may be given as the diagnosis. In other people suffering from mitochondrial disease, CPEO occurs...
15 KB (1,759 words) - 21:43, 12 August 2023
temporarily required. In rare chronic forms of lactic acidosis caused by mitochondrial disease, a specific diet or dichloroacetate may be used. The prognosis of...
24 KB (2,732 words) - 13:48, 23 August 2024