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Metachromatic leukodystrophy (MLD) rarely has its clinical onset in young adults, with a combination of cognitive and behavioural symptoms and peripheral neuropathy. Here we present an exceptional case with very late onset at 42 years of age and no c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb286dcc84d7ebd39c9f95509bc8899b
http://hdl.handle.net/11562/26630
http://hdl.handle.net/11562/26630