Pathogenic Mechanisms in Canavan Disease

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Date: 2014-01-13 12:12:17 Rare diseases Lipid storage disorders Leukodystrophies Canavan disease Paola Leone Gene delivery Chromosome 17 Canavan Hypotonia Health Biology Medicine		Pathogenic Mechanisms in Canavan Disease Add to Reading List Source URL: osp.od.nih.gov Download Document from Source Website File Size: 4,01 MB Share Document on Facebook

	Rare: abnormal gait, abnormal thinking, aggressive reaction, apathy, appetite increased, decreased libido, delusion, dementia, depersonalization, dysphasia, feeling strange, hypokinesia, hypotonia, hysteria, intoxicated DocID: 1rLN7 - View Document
	Congenital muscular dystrophies What is congenital muscular dystrophy? The congenital muscular dystrophies are a group of conditions which share early presentation and a common muscle pathology. Congenital means ‘from DocID: 1qbgq - View Document
	An Introductory Guide History Diagnosis Symptoms Treatments and Therapies Resources DocID: 1oQCk - View Document
	Patients should be taken with or nitazoxanide kaufen without food every four to six hours as needed. Symptoms of overdose may include ataxia, hypotonia, hypotension, hypnotic state, coma, cardiovascular depression, respi DocID: 1gmrA - View Document
	SureStep SMO I N D I C AT I O N S • Pronation • Low muscle tone (hypotonia) • Developmental delay • Delay in acquiring gross motor skills DocID: 1eyw6 - View Document