Case report Mitochondrial diseases show a broad phenotypic spectrum and are underdiagnosed. We present a 37-year-old woman referred to our neurology clinic after an incidental finding of bilateral caudate, lent
TEFMvariants impair mitochondrial transcription causing childhood-onset neurological disease Van Hauteet aldescribe autosomal recessive TEFM variants that impair mitochondrial transcription elongation and reduce the levels of promoter distal mitochondrial RNA transcripts, leading to heterogeneous mitochondrial diseases...
Mitochondrial diseases are caused by mutations in mitochondrial DNA inherited from the mother. Mitochondria are the part of the cell that produces the...Become a member and unlock all Study Answers Start today. Try it now Create an account Ask a question Our experts can ans...
What are the symptoms of pervasive developmental disorder? What are the symptoms of myelopathy? What are symptoms of achondroplasia? What are the symptoms of mitochondrial dysfunction? What are the first symptoms of Bell's palsy? What are the symptoms of Addison's disease?
Jaundice in Adults (Hyperbilirubinemia) K K BGSadmin 00 Kahlers disease (Multiple Myeloma) Unveiling the mysteries of Kahlers Disease: Explore groundbreaking research and treatment options for Multiple Myeloma in this comprehensive guide. Devamını Oku » ...
Prisma Flow Diagram visualizing the selection and filtering process of the conducted systematic literature search. (A) Studies investigating the role of gut microbiome in the link between inflammatory bowel disease and mental health; (B) Studies investigating pro-, pre- and synbiotic treatment in ment...
The aim of our study was to assess psychiatric symptoms in patients with genetically proven primary mutation of the mitochondrial DNA. 19 adults with known mitochondrial mutation (MT) have been assessed with the Stanford Health Assessment Questionnaire 2
Answer to: Discuss the causes, symptoms, and disorder names of mitochondrial disease. By signing up, you'll get thousands of step-by-step solutions...
This systematic review and meta-analysis addresses whether adults with persistent COVID-19 symptoms more than 3 months after SARS-CoV-2 infection (long
Wilson's disease is genetic and is inherited through autosomal recessive patterns. Wilson's disease is caused by an excess buildup of copper in a... Learn more about this topic: Copper in the Body | Function, Toxicity & Deficiency