Cargando…

A Clinical Diagnosis of Wiskott Aldrich Syndrome in an Ethiopian Boy with Recurrent Sinopulmonary Infections: A Case Report

BACKGROUND: Wiskott Aldrich syndrome is a primary immunodeficiency notable for eczema, recurrent infections, bleeding diathesis and microcytic thrombocytopenia. CASE: A 4½ year old boy presented with recurrent sinopulmonary infections, repeated treatment for severe eczema since infancy, thrombocytop...

Descripción completa

Detalles Bibliográficos
Autores principales:	Deribssa, Solomie Jebessa, Alemayehu, Tinsae
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Research and Publications Office of Jimma University 2020
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047228/ https://www.ncbi.nlm.nih.gov/pubmed/33883853 http://dx.doi.org/10.4314/ejhs.v30i6.26

Ejemplares similares

A First Case Report of DiGeorge Syndrome from Ethiopia Highlights Challenges in Identifying and Treating Children with Primary T-Cell Deficiencies in Low Resource Settings
por: Alemayehu, Tinsae, et al.
Publicado: (2020)

Unraveling the Repertoire in Wiskott–Aldrich Syndrome
por: Petersen, Sven H., et al.
Publicado: (2014)

Síndrome de Wiskott - Aldrich /
por: Tello Gabriel, Adriana

Wiskott–Aldrich syndrome: diagnosis, current management, and emerging treatments
por: Buchbinder, David, et al.
Publicado: (2014)

Assessment of Immature Platelet Fraction in the Diagnosis of Wiskott–Aldrich Syndrome
por: Sokolic, Robert, et al.
Publicado: (2015)

Autoimmunity in Wiskott–Aldrich Syndrome: An Unsolved Enigma
por: Catucci, Marco, et al.
Publicado: (2012)

Autoimmunity in Wiskott–Aldrich Syndrome: Updated Perspectives
por: Sudhakar, Murugan, et al.
Publicado: (2021)

Corneal ulceration and episcleritis associated with Wiskott–Aldrich syndrome
por: Zagelbaum, Bruce M., et al.
Publicado: (2016)

Wiskott-Aldrich Syndrome: New Perspectives in Pathogenesis and Management
por: Standen, G. R.
Publicado: (1988)

Confirmed diagnosis of classic Wiskott–Aldrich syndrome in East Africa: a case report
por: Kiputa, Mpokigwa, et al.
Publicado: (2022)

A First Report on Experience in Managing Infants with Congenital Toxoplasmosis in Ethiopia: Case Reports and a Review of Evaluation and Treatment
por: Alemayehu, Tinsae, et al.
Publicado: (2021)

T cell lines characterize events in the pathogenesis of the Wiskott- Aldrich syndrome
Publicado: (1992)

The Wiskott-Aldrich Syndrome: The Actin Cytoskeleton and Immune Cell Function
por: Blundell, Michael P., et al.
Publicado: (2010)

Wiskott-Aldrich syndrome proteins in the nucleus: aWASH with possibilities
por: Verboon, Jeffrey M, et al.
Publicado: (2015)

A Novel Mutation in a Patient with Wiskott-Aldrich Syndrome
por: Öncül, Yurday, et al.
Publicado: (2020)

Wiskott Aldrich syndrome: healthcare utilizations and disparities in transplant care
por: Agarwal, Nikki, et al.
Publicado: (2021)

Wiskott-Aldrich Syndrome Protein: Roles in Signal Transduction in T Cells
por: Ngoenkam, Jatuporn, et al.
Publicado: (2021)

Prolonged survival after splenectomy in Wiskott-Aldrich syndrome: a case report
por: Syrigos, Kostas N, et al.
Publicado: (2011)

Evolution of Highly Polymorphic T Cell Populations in Siblings with the Wiskott-Aldrich Syndrome
por: Lutskiy, Maxim I., et al.
Publicado: (2008)

Wiskott-Aldrich Syndrome (WAS) and Dedicator of Cytokinesis 8- (DOCK8) Deficiency
por: Albert, Michael H., et al.
Publicado: (2019)

Mechanisms of increased mitochondria-dependent necrosis in Wiskott-Aldrich syndrome platelets
por: Obydennyi, Sergey I., et al.
Publicado: (2020)

IL‐18: A potential inflammation biomarker in Wiskott–Aldrich syndrome
por: Rivers, Elizabeth, et al.
Publicado: (2021)

Wiskott–Aldrich syndrome: Oral findings and microbiota in children and review of the literature
por: Lucchese, Alessandra, et al.
Publicado: (2022)

Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India
por: Suri, Deepti, et al.
Publicado: (2021)

Altered O-glycan synthesis in lymphocytes from patients with Wiskott- Aldrich syndrome
Publicado: (1991)

Characterization of a human lymphocyte surface sialoglycoprotein that is defective in Wiskott-Aldrich syndrome
Publicado: (1984)

The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function
por: Locci, Michela, et al.
Publicado: (2009)

Genome editing for primary immunodeficiencies: A therapeutic perspective on Wiskott-Aldrich syndrome
por: Naseem, Asma, et al.
Publicado: (2022)

Wiskott-Aldrich syndrome protein forms nuclear condensates and regulates alternative splicing
por: Yuan, Baolei, et al.
Publicado: (2022)

Transcriptomic insights into the role of the spleen in a mouse model of Wiskott‑Aldrich syndrome
por: Liang, Fangfang, et al.
Publicado: (2022)

A novel genomic inversion in Wiskott-Aldrich–associated autoinflammation
por: Brigida, Immacolata, et al.
Publicado: (2016)

Wiskott–Aldrich syndrome that was initially diagnosed as immune thrombocytopenic purpura secondary to a cytomegalovirus infection
por: Kaneko, Ryota, et al.
Publicado: (2018)

A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection
por: Kaya, Zühre, et al.
Publicado: (2019)

A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report
por: Baharin, Mohd Farid, et al.
Publicado: (2016)

Persistent COVID-19 Infection in Wiskott-Aldrich Syndrome Cleared Following Therapeutic Vaccination: a Case Report
por: Bradley, Rachel E., et al.
Publicado: (2021)

Wiskott-Aldrich syndrome protein deficiency in B cells results in impaired peripheral homeostasis
por: Meyer-Bahlburg, Almut, et al.
Publicado: (2008)

The Chemotactic Defect in Wiskott-Aldrich Syndrome Macrophages Is Due to the Reduced Persistence of Directional Protrusions
por: Ishihara, Dan, et al.
Publicado: (2012)

Development of Central Nervous System Autoimmunity Is Impaired in the Absence of Wiskott-Aldrich Syndrome Protein
por: Bosticardo, Marita, et al.
Publicado: (2014)

Wiskott–Aldrich Syndrome protein deficiency perturbs the homeostasis of B-cell compartment in humans()
por: Castiello, Maria Carmina, et al.
Publicado: (2014)

Signal Integration during T Lymphocyte Activation and Function: Lessons from the Wiskott–Aldrich Syndrome
por: Cotta-de-Almeida, Vinicius, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_0kdj1urjol4ciesfqv6sltqkbo