III型白细胞粘附缺陷：原发性免疫缺陷与血小板功能缺陷的罕见关联

Q4 Medicine

Journal of Applied Hematology Pub Date : 2022-01-01 DOI:10.4103/joah.joah_43_21

Anand Krishnan Prakash

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引用次数: 0

摘要

白细胞粘附缺陷（LAD）III型是一种极为罕见的疾病，表现为严重感染和Glanzmann血栓衰弱样出血表型。一名2岁的男性儿童患有LAD III型，伴有复发性粘膜出血和相对较少的感染，以突出这一新颖的表现。描述了原发性免疫缺陷和血小板功能性疾病的罕见关联。

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Leukocyte adhesion defects Type III: A rare association of primary immunodeficiency and platelet functional defect

Leukocyte adhesion defect (LAD) Type III is an extremely rare disease, which presents with severe infections and a Glanzmann thrombasthenia-like bleeding phenotype. A 2-year-old male child with LAD Type III with recurrent mucosal bleeding and relatively few infections is presented to highlight this novel presentation. The rare association of primary immunodeficiency and platelet functional disease is described.

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来源期刊

Journal of Applied Hematology Medicine-Hematology

CiteScore

0.40

自引率

0.00%

发文量

审稿时长

24 weeks