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infantile neuroaxonal dystrophy |
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infantile neuroaxonal dystrophy [′in·fən‚tīl ¦nu̇·rō¦ak·sən·əl ′dis·trə·fē]
(medicine) A familial disease of the central nervous system occurring early in life and characterized by axonal swellings, arrested development, atrophy of the optic nerves, and eventual blindness. 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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