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infantile neuroaxonal dystrophy |
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infantile neuroaxonal dystrophy, progressive hereditary degenerative encephalopathy transmitted as an autosomal-recessive trait, beginning in infancy with muscular hypotonia and arrest of development in late infancy, followed by dementia, blindness, spasticity, and ataxia. Pathologically it is characterized by widespread focal swellings and degeneration of the axons with scattered globular bodies in the brain. Also called Seitelberger's disease. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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NBIA, PLA2G6-related |
NBHF NBHFM NBHGSF NBHH NBHHY NBHI NBHK NBHL NBHM NBHN NBHNC NBHOF NBHPP NBHRC NBHRN NBHS NBHTA NBHTC NBHTF NBHU NBHW NBI NBI NBI-NCFL NBIA NBIA, PLA2G6-related NBIAANBIAP NBIAS NBIC NBICA NBICF NBICS NBICU NBID NBIE NBIF NBIfAFG NBIFF NBIG NBII NBIIC NBIJ NBIL NBILP NBIM NBIMC NBIMCC NBIMF NBIMS | ||||||
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