نتایج جستجو برای: mitochondrial encephalomyopathy

تعداد نتایج: 132426  

Journal: :Human molecular genetics 2004
Yutaka Nishigaki Ramon Marti Michio Hirano

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive multisystem disorder associated with depletion, multiple deletions and site-specific point mutations of mitochondrial DNA (mtDNA). MNGIE is caused by loss-of-function mutations in the gene encoding thymidine phosphorylase (TP; endothelial cell growth factor 1). Deficiency of TP leads to dramatically elevated...

2015
Masaki Kodaira Hideyuki Hatakeyama Shinsuke Yuasa Tomohisa Seki Toru Egashira Shugo Tohyama Yusuke Kuroda Atsushi Tanaka Shinichiro Okata Hisayuki Hashimoto Dai Kusumoto Akira Kunitomi Makoto Takei Shin Kashimura Tomoyuki Suzuki Gakuto Yozu Masaya Shimojima Chikaaki Motoda Nozomi Hayashiji Yuki Saito Yu-ichi Goto Keiichi Fukuda

Mitochondrial diseases are heterogeneous disorders, caused by mitochondrial dysfunction. Mitochondria are not regulated solely by nuclear genomic DNA but by mitochondrial DNA. It is difficult to develop effective therapies for mitochondrial disease because of the lack of mitochondrial disease models. Mitochondrial myopathy, encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is...

Journal: :Genes 2021

Mitochondrial disorders, although heterogeneous, are traditionally described as conditions characterized by encephalomyopathy, hypotonia, and progressive postnatal organ failure. Here, we provide a systematic review of Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA), rare, unconventional mitochondrial disorder which presents developmental disease; its main clinical features incl...

Journal: :Molecular syndromology 2014
Luis C López Marta Luna-Sánchez Laura García-Corzo Catarina M Quinzii Michio Hirano

Primary coenzyme Q10 (CoQ10) deficiency is a rare mitochondrial disorder associated with 5 major clinical phenotypes: (1) encephalomyopathy, (2) severe infantile multisystemic disease, (3) cerebellar ataxia, (4) isolated myopathy, and (5) steroid-resistant nephrotic syndrome. Growth retardation, deafness and hearing loss have also been described in CoQ10-deficient patients. This heterogeneity i...

2015
Vianey Q. Casarez Acsa M. Zavala Pascal Owusu-Agyemang Katherine Hagan

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive disorder associated with deficiency of thymidine phosphorylase (TP). Associated manifestations include visual and hearing impairments, peripheral neuropathies, leukoencephalopathy, and malnutrition from concomitant gastrointestinal dysmotility and pseudoobstruction. Given the altered metabolic state in these...

2014
S Dindyal K Mistry N Angamuthu G Smith D Hilton Arumugam P J Mathew

MELAS (mitochondrial cytopathy, encephalomyopathy, lactic acidosis and stroke-like episodes) is a syndrome in which signs and symptoms of gastrointestinal disease are uncommon if not rare. We describe the case of a young woman who presented as an acute surgical emergency, diagnosed as toxic megacolon necessitating an emergency total colectomy. MELAS syndrome was suspected postoperatively owing ...

2015
Sivakumar Gopalswamy Joseph Mathew

MELAS syndrome (mitochondrial cytopathy, encephalomyopathy, lactic acidosis and stroke like episodes) is a syndrome in which signs and symptoms of gastro-intestinal disease are uncommon, if not rare. We describe a young female patient who presented as an acute surgical emergency, diagnosed as toxic mega colon necessitating an emergency total colectomy; the diagnosis of MELAS syndrome was made p...

Journal: :The Ochsner journal 2009
Christiane Koszka

Friedrich Nietzsche was one of the most influential and profound German philosophers. After prolonged illness, he died at the age of 55 in Weimar, Germany. The interest in his medical biography has always been strong while the cause of his illness and death has remained a mystery, intriguing philosophers as well as physicians. The diagnosis of syphilis proposed in the 19th century has been cont...

2016
Hanife Karakaya Kabukcu Nursel Sahin Ibrahim Basarici Ozan Erbasan

Central venous catheterization as a frequent routine clinical procedure may have significant complications. Mechanical complications may occur during catheter placement, whereas thromboembolic and infectious complications can be seen during follow-up. Total parenteral nutrition (TPN) associated central venous catheterizations may result in early mechanical complications and thrombotic and infec...

2011
Olga Z. Karicheva Olga A. Kolesnikova Tom Schirtz Mikhail Y. Vysokikh Anne-Marie Mager-Heckel Anne Lombès Abdeldjalil Boucheham Igor A. Krasheninnikov Robert P. Martin Nina Entelis Ivan Tarassov

Mutations in human mitochondrial DNA are often associated with incurable human neuromuscular diseases. Among these mutations, an important number have been identified in tRNA genes, including 29 in the gene MT-TL1 coding for the tRNA(Leu(UUR)). The m.3243A>G mutation was described as the major cause of the MELAS syndrome (mitochondrial encephalomyopathy with lactic acidosis and stroke-like epis...

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