Macrothrombocytopenia With Döhle Body-Like Granulocyte Inclusions: A Case Report of May-Hegglin Anomaly in a 33-Year-Old White Woman With an Update on the Molecular Findings ofMYH9-Related Disease
Author:
Publisher
Oxford University Press (OUP)
Subject
Biochemistry, medical,Clinical Biochemistry
Link
http://academic.oup.com/labmed/article-pdf/47/3/246/14141796/lmw033.pdf
Reference18 articles.
1. MYH9-Related Platelet Disorders
2. Successful Renal Transplantation in MYH9-Related Disorder With Severe Macrothrombocytopenia: First Report in Korea
3. It is not always immune thrombocytopenia: a case of MYH9-related platelet disorder caused by a novel mutation
4. The first two cases of MYH9 disorders in Thailand: an international collaborative study
5. MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations
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1. Successful hematopoietic stem cell transplantation in MYH9‐related congenital thrombocytopenia;Pediatric Blood & Cancer;2024-06-26
2. Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report;Transfusion and Apheresis Science;2023-08
3. The surgical management of a patient with chronic renal failure and macrothrombocytopenia related to the MYH9 gene mutation: A case report;Special Care in Dentistry;2022-05-10
4. The May-Hegglin anomaly: a rare cause of a common complaint;BMJ Case Reports;2021-03
5. Hereditary Coagulation Disorders;Essentials of Blood Product Management in Anesthesia Practice;2021
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