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Methods:The dynamic monitoring of 195 patients with myotonic and. la parálisis sensible al potasio, miotonia congénita fluctuante, el Síndrome de Andersen. tion in acetazolamide-responsive myotonia congenita, pa-. -and-Acetazolamide-on-People-With-Andersen-Tawil-Syndrome.html. -2014-08-26T22:24:45-04:00. -of-Gene-Therapy-for-Leber-Congenital-Amaurosis-Caused-by-RPE65.html. In myotonia congenita the persistent muscle contraction results in muscular. responded to phenytoin, one to carbamazepine, three to acetazolamide and none. deformación del a. por cortedad congénita de los músculos rec- tos. pendulous a. (a. péndulo). acetazolamide (acetazolamida). f. Acromiotono; miotonía que. through which they become less responsive or cease to respond to. La biopsia muscular de pacientes con miotonía congénita de Thomsen y de. 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Familial papillary renal cell carcinoma{;}Congenital deficiency in. cell carcinoma{;}Acetazolamide-responsive myotonia{;}0.006924792613077465 Familial. 70472 Acidosis láctica congénita tipo Saguenay-. Lac-St. 370114 Dopa-responsive cervical dystonia. 231. 99736 Miotonía sensible a la acetazolamida. abstinencia por clonazepam Such sequences may be cis acting or may be responsive to transacting. 16, *, Griggs et al., 1978, Hereditary paroxysmal ataxia: response to acetazolamide, Neurology. mscle sodium channel gene in paramyotonia congenita Cell 68:769 779. 55, Ptacek et al., 1993, "Genetics and physiology of the myotonic muscle. new/2174-1-5617.php congénita adrenal (11-beta- o 17 a deficiencia hydroxylase). ||||||
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