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Homocystinuria: A rare condition presenting as stroke and megaloblastic anemia

Homocystinuria is an inborn error of amino acid metabolism in which homocystine accumulates in the blood and produces a slowly evolving clinical syndrome. We are presenting a case of a 4-year-old female child who presented to us with stroke and also had megaloblastic anemia. She was diagnosed as hav...

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Detalhes bibliográficos
Main Authors: Bhardwaj, Parveen, Sharma, Ravi, Sharma, Minoo
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3087990/
https://ncbi.nlm.nih.gov/pubmed/21559159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.76110
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