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This Concept Map, created with IHMC CmapTools, has information related to: mark davis_a7 jen, motor skill lag including pseudohypertrophy and woody feeling, Muscular Dystrophy with recommended treatment including Referral to pediatric neurologist and Muscular Dystrophy clinic, western blot showed almost complete absence of dystrophin (ɛ% of normal), Muscular Dystrophy with recommended treatment including Novel Therapies, X-linked inheritance of single base pair mutation of Xp21.1-2, Duchenne's Muscular Dystrophy based on Diagnostic studies, premature stop codon and an altered genetic sequence, Diagnostic studies including EKG, single base pair mutation of Xp21.1-2 causes premature stop codon, motor skill lag including weak right foot that turns out during ambulation, Novel Therapies such as Induced Exon skipping, Mark Davis family history of mild developmental delay (mother), Mark Davis is a 6 y/o Caucasian Male, Normal sinus rhythm with tall right precordial R waves with an increased R/S ratio and deep Q waves in I, AVL and V5-V6. indicative of cardiomyopathy, developmental delays in physical coordination manifests as motor skill lag, calcium sensitive enzymes such as ATPase, translation promoting protein with residual dystrophin function, calcium signaling activates calcium sensitive enzymes, Mark Davis family history of myocardial infarction, motor skill lag including positive Gower's sign