• Thumbnail for Mitochondrial DNA depletion syndrome
    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) - 15:09, 27 October 2024
  • Thumbnail for Mitochondrial myopathy
    in TK2 deficiency (Mitochondrial DNA depletion syndrome 2 myopathic type). Avoiding physically stressful situations that deplete glycogen reserves, such...
    43 KB (3,582 words) - 16:26, 16 October 2024
  • Thumbnail for Mitochondrial disease
    intolerance MELAS syndrome, mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes Mitochondrial DNA depletion syndrome Conditions such...
    32 KB (3,475 words) - 18:22, 1 November 2024
  • Thumbnail for Mitochondrial neurogastrointestinal encephalopathy syndrome
    syndrome). The disease presents in childhood, but often goes unnoticed for decades. Unlike typical mitochondrial diseases caused by mitochondrial DNA...
    9 KB (800 words) - 15:08, 27 October 2024
  • 2016 – 28 July 2017), an infant boy from London, born with mitochondrial DNA depletion syndrome (MDDS), a rare genetic disorder that causes progressive brain...
    101 KB (12,457 words) - 12:14, 15 October 2024
  • Thumbnail for MELAS syndrome
    in the mitochondrial genome which is inherited purely from the female parent. The most common MELAS mutation is mitochondrial mutation, mtDNA, referred...
    17 KB (1,797 words) - 22:06, 11 October 2024
  • Thumbnail for Plagiocephaly
    Joubert syndrome 1 Kleefstra syndrome 2 Langer-Giedion syndrome Microphthalmia with brain and digit anomalies Mitochondrial DNA depletion syndrome 13 Muenke...
    18 KB (1,736 words) - 03:33, 30 July 2024
  • degeneration (AMD) Marfan's syndrome (MFS) Some mitochondrial myopathies Mitochondrial DNA depletion syndrome Mueller–Weiss syndrome Multiple sclerosis (MS)...
    16 KB (1,643 words) - 13:32, 29 July 2024
  • Mismatch repair cancer syndrome Mitochondrial DNA depletion syndrome Mitochondrial neurogastrointestinal encephalopathy syndrome Mitral valve prolapse...
    42 KB (4,068 words) - 16:56, 1 November 2024
  • Thumbnail for Multiple sclerosis
    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,...
    170 KB (18,177 words) - 09:23, 7 November 2024
  • Thumbnail for SUCLA2
    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...
    14 KB (1,745 words) - 05:53, 12 January 2024
  • Thumbnail for Narrow face
    Knobloch syndrome Marfan syndrome Mitochondrial DNA depletion syndrome 13 Nance-Horan syndrome Oculofaciocardiodental syndrome Otofaciocervical syndrome 1 Proximal...
    4 KB (224 words) - 07:14, 15 April 2024
  • Thumbnail for Methylmalonic acidemias
    homocystinuria, type cblD". Orphanet. Retrieved 2024-04-27. "Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria". Orphanet...
    48 KB (4,435 words) - 15:54, 30 October 2024
  • ES, Wong LJ (July 2010). "Quantitative evaluation of the mitochondrial DNA depletion syndrome". Clinical Chemistry. 56 (7): 1119–27. doi:10.1373/clinchem...
    55 KB (5,349 words) - 01:10, 23 October 2024
  • Thumbnail for Kinase
    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...
    34 KB (3,807 words) - 07:35, 29 October 2024
  • Thumbnail for Mohr–Tranebjærg syndrome
    Arts syndrome Autosomal recessive nonsyndromic sensorineural deafness type DFNB Friedreich ataxia MELAS syndrome Mitochondrial DNA depletion syndrome (encephalomyopathic...
    9 KB (1,034 words) - 19:10, 12 October 2023
  • Mesothelioma Methylmalonic acidemia Mitiglinide Mitochondrial DNA depletion syndrome, hepatocerebral form Mitochondrial trifunctional protein deficiency Multiple...
    21 KB (1,265 words) - 01:46, 22 December 2023
  • Thumbnail for AGK (gene)
    lysophosphatidic acids. Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10. Diseases associated with AGK include cataracts and cardiomyopathy...
    11 KB (1,381 words) - 06:22, 10 June 2024
  • syndrome Gyrate atrophy of choroid and retina Hydrolethalus syndrome 1 Infantile-onset spinocerebellar ataxia (Mitochondrial DNA depletion syndrome 7)...
    13 KB (1,459 words) - 14:53, 10 October 2024
  • Thumbnail for Thymidine kinase 2, mitochondrial
    required for mitochondrial DNA synthesis. Mutations in this gene are associated with a myopathic form of mitochondrial DNA depletion syndrome. Alternate...
    1 KB (193 words) - 14:52, 20 January 2024
  • Thumbnail for Organic anion transporter 1
    decrease in mitochondrial respiration and an increase in mitochondrial mass in fat cells. Stavudine also causes severe mitochondrial DNA depletion. Combining...
    22 KB (2,503 words) - 00:44, 4 March 2023
  • can affect metabolism and mitochondrial function in newborns with ZTTK syndrome. Metabolic screening confirmed mitochondrial dysfunction and O-glycosylation...
    25 KB (2,954 words) - 11:16, 11 May 2024
  • 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...
    97 KB (11,101 words) - 11:45, 3 September 2024
  • Mal de debarquement (MdDS), a rare neurological condition Mitochondrial DNA depletion syndrome, a group of autosomal recessive disorders MDD (disambiguation)...
    1 KB (68 words) - 14:27, 6 March 2021
  • Thumbnail for DGUOK
    gene. Mutations in this gene have been linked to inherited mitochondrial DNA depletion syndromes, neonatal liver failure, nystagmus and hypotonia. GRCh38:...
    8 KB (1,023 words) - 22:39, 18 August 2023
  • Thumbnail for RRM2B
    mutated. Abnormalities in this gene are one of the causes of mitochondrial DNA depletion syndrome (MDDS). Neonatal hypotonia, developmental delay, encephalopathy...
    12 KB (1,508 words) - 14:11, 2 November 2024
  • Thumbnail for Gitelman syndrome
    the mitochondrial DNA can also cause a Gitelman-like syndrome. These homoplasmic mitochondrial DNA mutations are maternally inherited. To treat the symptoms...
    28 KB (2,941 words) - 15:49, 11 October 2024
  • 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...
    81 KB (4,147 words) - 04:14, 4 October 2024
  • Thumbnail for POLG
    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,...
    15 KB (1,864 words) - 21:00, 1 May 2024
  • Thumbnail for Lupus
    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