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Familial Pelger–Huet Anomaly
Pelger–Huet anomaly is usually autosomal dominant, although it is likely that new mutations are common. This condition is characterized by granulocytes that are either bilobed or completely unsegmented. Here is a report of a 46 year old Indian lady who presented with fever to the hospital and on eva...
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| Publicado no: | Indian J Hematol Blood Transfus |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer India
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4925487/ https://ncbi.nlm.nih.gov/pubmed/27408433 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-015-0508-3 |
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