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Article

First report of successful stem cell transplantation in a patient with sickle cell hemoglobin D disease.

Journal of pediatric hematology/oncology - 1 Jul 2010

Hamidieh Amir Ali, Jalili Mahdi, Khojasteh Omid, Ghavamzadeh Ardeshir

Abstract excerpt

Sickle cell hemoglobin D disease is a rare variant of sickle cell disease. Affected patients suffer from episodes of acute exacerbation of clinical course with a wide range of manifestations such as acute chest syndrome, stroke, painful vaso-occlusive crises, acute sequestration crises, joint necrosis, organ failure, infections, and temporary aplastic crises, collectively called sickling crises. Conventional...

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Identifiers

PMID: 20502357
DOI: 10.1097/MPH.0b013e3181df614b

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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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