دورية أكاديمية

Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease?

التفاصيل البيبلوغرافية
العنوان: Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease?
المؤلفون: González-Freire, Marta, Santiago Dorrego, Catalina, Gómez Gallego, Félix, Pérez Ruiz, Margarita, Foster, Carl, Arenas, Joaquín, Lucía Mulas, Alejandro
سنة النشر: 2009
المجموعة: Universidad Europea: ABACUS
مصطلحات موضوعية: Genetic Predisposition To Disease/*Genetics, Glycogen Storage Disease Type V/*Genetics, Mutation/*Genetics, Myostatin/*Genetics, Amp Deaminase/Genetics, Dna Mutational Analysis, Exercise Tolerance/Genetics, Female, Genetic Variation/Genetics, Genotype, Glycogen/Metabolism, Glycogen Storage Disease Type V/Metabolism, Glycogen Storage Disease Type V/Physiopathology, Heterozygote, Humans, Muscle Weakness/Genetics, Muscle, Skeletal/Metabolism, Skeletal/Physiopathology, Peptidyl-Dipeptidase A/Genetics, Phenotype, Respiratory Insufficiency/Genetics, Enfermedad nutricional, Deporte, Tratamiento médico
الوصف: There is individual variability in the clinical manifestation of McArdle disease, with women generally being more severely affected than men. We compared clinical presentation and exercise capacity between (i) four women with McArdle disease (aged 17, 36, 42 and 70 years) who were also carriers of the K153R variant in the myostatin (GDF-8) gene and in (ii) four women with this disorder matched forage (16, 33, 40 and 69 years), lifestyle, and documented genotype modulators of this disease (ACE, AMPD1 and ACTN3), who did not carry the myostatin variant. Except in the youngest patient, clinical severity was higher in K153R carriers than in their K/K(2) controls (aged 33, 40 and 46 years). Peak cardiorespiratory capacity was very low (< or = 13 mLO(2)/kg/min) in all K153R carriers. ; 2.977 JCR (2009) Q2, 49/167 Clinical neurology, 105/231 Neurosciences ; UEM
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 18732364
العلاقة: González-Freire, M., Santiago-Dorrego, C., Gómez-Gallego, F., Pérez-Ruiz, M., Foster, C., Arenas, J., & Lucía-Mulas, A. (2009). Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease? Neuromuscular Disorders, 19(3), 220-222.; http://hdl.handle.net/11268/1120Test
DOI: 10.1016/j.nmd.2009.01.001
الإتاحة: https://doi.org/10.1016/j.nmd.2009.01.001Test
http://hdl.handle.net/11268/1120Test
حقوق: closedAccess
رقم الانضمام: edsbas.FC69F611
قاعدة البيانات: BASE
الوصف
تدمد:18732364
DOI:10.1016/j.nmd.2009.01.001