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Glanzmann's thrombasthenia: a rare bleeding disorder in a Nigerian girl
INTRODUCTION: Glanzmann's Thrombasthenia (GT) is a rare autosomal recessive bleeding disorder due to defective platelet membrane glycoprotein GP IIb/IIIa (integrin αIIbβ3). The prevalence is estimated at 1:1,000,000 and it is commonly seen in areas where consanguinity is high. CASE PRESENTATION...
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| Vydáno v: | Afr Health Sci |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Makerere Medical School
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7609079/ https://ncbi.nlm.nih.gov/pubmed/33163040 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4314/ahs.v20i2.27 |
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