نتایج جستجو برای: a3243g mutation

تعداد نتایج: 291433  

Many kinds of mutations in mitochondrial (mt) DNA have been reported to be related to the development of Diabetes Mellitus (DM), this type of diabetes has also been shown to be influenced by other genetic factors and/or environmental factors. Among them, tRNALeu(UUR) and its adjacent mtDNA NADH dehydrogenase subunit 1(ND1) region within the mt genome are linked to high susceptibility to DM. A p...

Journal: :Clinical endocrinology 2009
Tricia M M Tan Carmela Caputo Francesco Medici Alidz L Pambakian Anne Dornhorst Karim Meeran Graham R Williams Bernard Khoo

The mitochondrial DNA mutation MTTL1 A3243G causes MELAS syndrome (Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-like episodes). The A3243G mutation is also associated with variable endocrinopathies. We describe 2 case histories of patients with the A3243G mutation. The first patient presented with diabetes and uncontrolled Graves’ thyrotoxicosis in association with a strokelike epis...

Journal: :Endocrine journal 2008
Yutaka Takahashi Keiji Iida Ryoko Takeno Riko Kitazawa Sohei Kitazawa Hidetsuna Kitamura Yoshio Fujioka Hiroyuki Yamada Fumio Kanda Shigeo Ohta Kiyomi Nishimaki Masayo Fujimoto Takeshi Kondo Genzo Iguchi Kentaro Takahashi Hidesuke Kaji Yasuhiko Okimura Kazuo Chihara

Mitochondrial diabetes is characterized by diabetes and hearing loss in maternal transmission with a heteroplasmic A3243G mutation in the mitochondrial gene. In patients with the mutation, it has been reported that hepatic involvement is rarely observed. We demonstrated a case of hypertrophic cardiomyopathy and hepatic failure with mitochondrial diabetes. To clarify the pathogenesis we analyzed...

Journal: :Archives of neurology 2007
Douglas M Sproule Petra Kaufmann Kristen Engelstad Thomas J Starc Allan J Hordof Darryl C De Vivo

BACKGROUND Tissues with high energy demands, such as the heart, are susceptible to the effects of mitochondrial DNA point mutations. OBJECTIVE To investigate the frequency of Wolff-Parkinson-White (WPW) syndrome among a phenotypically and genotypically homogeneous cohort of patients with MELAS (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes) and the A3243G mutation mos...

Journal: :Clinical chemistry 2004
Michiyo Urata Yui Wada Sang Ho Kim Worawan Chumpia Yuzo Kayamori Naotaka Hamasaki Dongchon Kang

BACKGROUND The A3243G mutation of mitochondrial DNA (mtDNA) is involved in many common diseases, including diabetes mellitus and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS). For detection of this mutation, allele-specific PCR is highly sensitive but requires strict control of PCR conditions; it thus is not adequate for a routine clinical test. We aimed ...

Journal: :Diabetes 2004
J Antonie Maassen Leen M 'T Hart Einar Van Essen Rob J Heine Giel Nijpels Roshan S Jahangir Tafrechi Anton K Raap George M C Janssen Herman H P J Lemkes

Mutations in mitochondrial DNA (mtDNA) associate with various disease states. A few mtDNA mutations strongly associate with diabetes, with the most common mutation being the A3243G mutation in the mitochondrial DNA-encoded tRNA(Leu,UUR) gene. This article describes clinical characteristics of mitochondrial diabetes and its molecular diagnosis. Furthermore, it outlines recent developments in the...

Journal: :Clinical chemistry 2004
Ren-Kui Bai Lee-Jun C Wong

BACKGROUND The A3243G mitochondrial tRNA leu(UUR) point mutation causes mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, the most common mitochondrial DNA (mtDNA) disorder, and is also found in patients with maternally inherited diabetes and deafness syndrome (MIDD). To correlate disease manifestation with mutation loads, it is necessary to mea...

Journal: :The Laryngoscope 2011
Shinichi Iwasaki Naoya Egami Chisato Fujimoto Yasuhiro Chihara Munetaka Ushio Akinori Kashio Tatsuya Yamasoba

OBJECTIVES/HYPOTHESIS To evaluate vestibular function in patients with the mitochondrial A3243G mutation. STUDY DESIGN Data from patients with the A3243G mutation attending an academic tertiary referral center were prospectively recorded. METHODS The clinical histories of 13 unrelated patients with the mitochondrial A3243G mutation (six mitochondrial encephalomyopathy, lactic acidosis, and ...

2011
Maryam Wahid Abdul Khaliq Naveed

Background:. A3243G mutation in tRNA Leu (UUR) leads to a specific clinical syndrome characterized by diabetes and sensorineural hearing defect, hence called as “Maternally Inherited Diabetes and Deafness (MIDD)”.. Methods: The study was retrospective, analytical case control study. Non probability convenient sampling technique was used. Subjects were divided into two groups. Thirty-nine patien...

Journal: :Developmental Medicine & Child Neurology 2007

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید