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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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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications
2010
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| Konular: | |
| Online Erişim: | 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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