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...
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in TK2 deficiency (Mitochondrial DNA depletion syndrome 2 myopathic type). Avoiding physically stressful situations that deplete glycogen reserves, such...
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intolerance MELAS syndrome, mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes Mitochondrial DNA depletion syndrome Conditions such...
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syndrome). The disease presents in childhood, but often goes unnoticed for decades. Unlike typical mitochondrial diseases caused by mitochondrial DNA...
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2016 – 28 July 2017), an infant boy from London, born with mitochondrial DNA depletion syndrome (MDDS), a rare genetic disorder that causes progressive brain...
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in the mitochondrial genome which is inherited purely from the female parent. The most common MELAS mutation is mitochondrial mutation, mtDNA, referred...
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Plagiocephaly (redirect from Flat head syndrome)
Joubert syndrome 1 Kleefstra syndrome 2 Langer-Giedion syndrome Microphthalmia with brain and digit anomalies Mitochondrial DNA depletion syndrome 13 Muenke...
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degeneration (AMD) Marfan's syndrome (MFS) Some mitochondrial myopathies Mitochondrial DNA depletion syndrome Mueller–Weiss syndrome Multiple sclerosis (MS)...
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Mismatch repair cancer syndrome Mitochondrial DNA depletion syndrome Mitochondrial neurogastrointestinal encephalopathy syndrome Mitral valve prolapse...
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healthcare. The condition begins in 85% of cases as a clinically isolated syndrome (CIS) over a number of days with 45% having motor or sensory problems,...
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succinate. Defects in this gene are a cause of myopathic mitochondrial DNA depletion syndrome. A pseudogene of this gene has been found on chromosome 6...
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Narrow face (section Syndromes (conditions))
Knobloch syndrome Marfan syndrome Mitochondrial DNA depletion syndrome 13 Nance-Horan syndrome Oculofaciocardiodental syndrome Otofaciocervical syndrome 1 Proximal...
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homocystinuria, type cblD". Orphanet. Retrieved 2024-04-27. "Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria". Orphanet...
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ES, Wong LJ (July 2010). "Quantitative evaluation of the mitochondrial DNA depletion syndrome". Clinical Chemistry. 56 (7): 1119–27. doi:10.1373/clinchem...
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in the thymidine kinase gene may have a certain type of mitochondrial DNA depletion syndrome, a disease that leads to death in early childhood. Wikimedia...
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Arts syndrome Autosomal recessive nonsyndromic sensorineural deafness type DFNB Friedreich ataxia MELAS syndrome Mitochondrial DNA depletion syndrome (encephalomyopathic...
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Mesothelioma Methylmalonic acidemia Mitiglinide Mitochondrial DNA depletion syndrome, hepatocerebral form Mitochondrial trifunctional protein deficiency Multiple...
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lysophosphatidic acids. Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10. Diseases associated with AGK include cataracts and cardiomyopathy...
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syndrome Gyrate atrophy of choroid and retina Hydrolethalus syndrome 1 Infantile-onset spinocerebellar ataxia (Mitochondrial DNA depletion syndrome 7)...
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required for mitochondrial DNA synthesis. Mutations in this gene are associated with a myopathic form of mitochondrial DNA depletion syndrome. Alternate...
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Organic anion transporter 1 (redirect from Iatrogenic Fanconi syndrome)
decrease in mitochondrial respiration and an increase in mitochondrial mass in fat cells. Stavudine also causes severe mitochondrial DNA depletion. Combining...
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can affect metabolism and mitochondrial function in newborns with ZTTK syndrome. Metabolic screening confirmed mitochondrial dysfunction and O-glycosylation...
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context is a DNA alteration that has an abnormal structure. Although both mitochondrial and nuclear DNA damage can contribute to aging, nuclear DNA is the main...
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Mal de debarquement (MdDS), a rare neurological condition Mitochondrial DNA depletion syndrome, a group of autosomal recessive disorders MDD (disambiguation)...
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gene. Mutations in this gene have been linked to inherited mitochondrial DNA depletion syndromes, neonatal liver failure, nystagmus and hypotonia. GRCh38:...
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mutated. Abnormalities in this gene are one of the causes of mitochondrial DNA depletion syndrome (MDDS). Neonatal hypotonia, developmental delay, encephalopathy...
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the mitochondrial DNA can also cause a Gitelman-like syndrome. These homoplasmic mitochondrial DNA mutations are maternally inherited. To treat the symptoms...
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in to investigate after a father (Joe Tapper) kidnaps his mitochondrial DNA depletion syndrome-affected infant. When the father is found, he says he wants...
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POLG (redirect from DNA polymerase gamma)
DNA polymerase subunit gamma (POLG or POLG1) is an enzyme that in humans is encoded by the POLG gene. Mitochondrial DNA polymerase is heterotrimeric,...
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Lupus (redirect from Osler-Libman-Sacks syndrome)
death, is increased in T lymphocytes, due to mitochondrial dysfunction, oxidative stress, and depletion of ATP. Impaired clearance of dying cells is a...
129 KB (14,190 words) - 06:36, 19 October 2024