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Publikováno v:
SAGE Open Medical Case Reports, Vol 12 (2024)
May-Hegglin anomaly (MHA) is a rare autosomal dominant disease associated with a mutation in the MYH-9 gene. It is characterized by macrothrombocytopenia and neutrophils with abnormal cytoplasmic inclusions. Clinical features of this disease include
Externí odkaz:
https://doaj.org/article/edddac8dcab245b3b0e52a3354dfe31a
