Anomalia de Pelger-Huët: um relato de caso pediátrico

The Pelger-Huët anomaly (PHA) is a benign, hereditary, usually autosomal dominant condition characterized by bilobulated or completely non-segmented granulocytes and excessive chromatin aggregation that can be mistaken for band cells. PHA is a condition still poorly investigated in the medical lite...

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Main Authors: Caroline Mundel (Author), Irides Aparecida Cavalari (Author), Ana Paula Vieira (Author), Franciele Ani Follador (Author), Guilherme Welter Wendt (Author), Lirane Elize Defante Ferreto (Author)
Format: Knjiga
Izdano: Sociedade Brasileira de Pediatria, 2022-12-01T00:00:00Z.
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