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: | , , , , , |
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| Format: | Book |
| Published: |
Sociedade Brasileira de Pediatria,
2022-12-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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