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Severe Prekallikrein Deficiency Associated with Low Level of Factor XII: A Case Report
Hereditary deficiency of plasma prekallikrein (PPK) is a rare autosomal recessive disease. The affected patients are often asymptomatic and diagnosed incidentally during preoperative investigations or during hospitalization by isolated prolongation of activated partial thromboplastin time (aPTT). In...
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| 出版年: | Iran J Pathol |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Iranian Society of Pathology
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8298060/ https://ncbi.nlm.nih.gov/pubmed/34306130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.30699/IJP.2020.131638.2463 |
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