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Article

The diagnostic protocol for hereditary spherocytosis-2021 update.

Journal of clinical laboratory analysis - 1 Dec 2021

Wu Yangyang, Liao Lin, Lin Faquan

Abstract excerpt

BACKGROUND: Hereditary spherocytosis (HS), a commonly encountered hereditary hemolytic disease, is mostly inherited in an autosomal dominant manner. The clinical manifestations in patients with HS show obvious heterogeneity. Moreover, the sensitivity or specificity of some HS diagnostic tests are not ideal and may easily result in misdiagnosis or missed diagnosis in some patients. The objective of this study was...

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Share to Anemia, Hemolytic, Autoimmune
Share to Diagnosis, Differential
Share to Diagnostic Errors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Erythrocyte Indices

Share to Glucosephosphate Dehydrogenase Deficiency

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Share to Spherocytosis, Hereditary

Source

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Identifiers

PMID: 34689357
DOI: 10.1002/jcla.24034
PMCID: PMC8649336

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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