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Hermansky–Pudlak syndrome in pregnancy: A case report
Hermansky–Pudlak syndrome is a rare autosomal recessive disorder estimated to affect 1 in 500,000 to 1,000,000 individuals worldwide. Clinically, it presents as oculocutaneous albinism combined with bleeding diathesis. This is due to the absence of dense bodies in platelets causing a delayed seconda...
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| Vydáno v: | Obstet Med |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5089347/ https://ncbi.nlm.nih.gov/pubmed/27829879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1753495X16662580 |
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