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Publikováno v:
Journal of Neurological Disorders.
Alkaptonuria is a rare metabolic disease caused by deficiency of homogentisic acid oxidase and characterized by bluish-black discoloration of cartilages and skin (ochronosis). Discal herniation requiring surgery is unusual in alkaptonuria, with only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1f234200ca6d38db42e0e06ac8e09a9
https://doi.org/10.4172/2329-6895.1000253
https://doi.org/10.4172/2329-6895.1000253
