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This Concept Map, created with IHMC CmapTools, has information related to: mark davis_a7, Mark Davis family history of myocardial infarction, transcript stability allowing for translation, altered genetic sequence leads to transcirption of altered mRNA, EKG shows 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., Clusters of necrotic and regenerating muscle fibers, severe proliferation of fibrous, fatty connective tissue with mononuclear inflammatory infiltrates Characteristic of Muscular Dystrophy, motor skill lag including weak right foot that turns out during ambulation, Muscular Dystrophy which presents as pseudohypertrophy and woody feeling, motor skill lag including positive Babinski sign (down-going bilaterally), Diagnostic studies includingEKG EKG, motor skill lag including hip girdle stength 3/5-4/5, Mark Davis presenting with poor growth, Muscular Dystrophy with recommended treatment including Novel Therapies, parents and paternal grandmother no history of consanguinity or neuromuscular disorders, motor skill lag including pseudohypertrophy and woody feeling, Duchenne's Muscular Dystrophy based on Diagnostic studies, Diagnostic studies using Muscle Biopsy, Mark Davis family history of Maternal uncle died in his teens - cause unknown, developmental delays in physical coordination appearing with Cranial Nerves II-XII intact, cardiomyopathy Characteristic of Muscular Dystrophy, open reading frame maintains transcript stability