Wiskott-Aldrich Syndrome Misdiagnosed as Immune Thrombocytopenic Purpura: A Case Report-Reference-Cited by-同舟云学术

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Wiskott-Aldrich Syndrome Misdiagnosed as Immune Thrombocytopenic Purpura: A Case Report

Published:2018-04 Issue:3 Volume:40 Page:240-242
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Karalexi Maria A.,Tzanoudaki Marianna,Fryganas Andreas,Gkergki Alexia,Spyropoulou Dora,Papadopoulou Anna,Papaevangelou Vassiliki,Petrocheilos Ioannis

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Wiskott-Aldrich syndrome: diagnosis, clinical and laboratory manifestations, and treatment;Ochs;Biol Blood Marrow Transplant,2009

2. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options;Albert;Blood,2010

3. Thrombocytopenic syndromes masquerading as childhood immune thrombocytopenic purpura;Bryant;Clin Pediatr,2011

4. The incidence of immune thrombocytopenic purpura in children and adults: a critical review of published reports;Terrell;Am J Hematol,2010

5. Confirming or excluding the diagnosis of Wiskott-Aldrich syndrome in children with thrombocytopenia of an unknown etiology;Ariga;J Pediatr Hematol/Oncol,2004

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Normal mean platelet volume and thrombocytopenia: It may still be Wiskott–Aldrich syndrome;Pediatric Allergy and Immunology;2024-08

2. Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott–Aldrich syndrome;Orphanet Journal of Rare Diseases;2022-12-22

3. A Review on Secondary Immune Thrombocytopenia in Malaysia;Healthcare;2021-12-26

4. Clinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience;Turkish Journal of Hematology;2020-11-19

5. When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura;Frontiers in Immunology;2019-07-09

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