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Hallervorden-Spatz Disease PDF Print E-mail
Written by Bhuvan Chand   
Tuesday, 29 September 2009 09:23

This is a rare neuroaxonal dystrophy, characterized by axonal spheroids, iron deposition, lewy body -like intraneuronal inclusions and neurofibrillary tangles

Symptoms

Symptoms usually appear in childhood,Progressive degeneration,Muscle contractions of the limbs, face,Muscle rigidity,Spasticity,Ataxia,Confusion,Disorientation,Seizures,Painful muscle spasms,Dysphasia,Mental retardation,Facial grimacing

Last Updated on Monday, 17 December 2012 20:15
 
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