نتایج جستجو برای: aldrich syndrome

تعداد نتایج: 623385  

Journal: :Journal of the Irish Medical Association 1969
B H Belohradsky C Griscelli H H Fundenberg W Marget

can occur, the observed improvement cannot necessarily b)e attributed to the transfer factor. However, in two patients repeated remissions consistently followed transfer factor administration on repeated occasions. This included freedom from infections, regression of splenomegaly, and clearing of eczema. An unexpected finding was a decrease in bleeding in 3 of the 10 patients who had bleeding. ...

Journal: :Voprosy gematologii/onkologii i immunopatologii v pediatrii 2022

This article discusses the role of electron microscopy in diagnosis and study morphological changes that cause platelet structural abnormalities a variety congenital diseases. Morphological can be divided into cytoskeleton, alpha dense granules, membrane abnormalities. Our paper describes ultrastructural defects Wiskott–Aldrich syndrome, MYH9-associated syndromes, gray Hermansky–Pudlak Paris–Tr...

Journal: :British Journal of Haematology 1998

Journal: :Japanese Journal of Clinical Immunology 2005

Journal: :Residência Pediátrica 2011

Journal: :Iranian journal of allergy, asthma, and immunology 2012
Sepideh Safaei Mohammad Reza Fazlollahi Masoud Houshmand Amir Ali Hamidieh Mohammad Hassan Bemanian Samin Alavi Farideh Mousavi Zahra Pourpak Mostafa Moin

Wiskott-Aldrich syndrome (WAS) is a life-threatening X-linked recessive immunodeficiency disease described as a clinical triad of thrombocytopenia, eczema, and recurrent infections, caused by mutations of the WAS protein (WASP) gene. The milder form of this disease is X-linked thrombocytopenia (XLT) that presents only as platelet abnormalities. Mutation analysis for 15 boys with Wiskott-Aldrich...

Journal: :Indian pediatrics 2014
Dejan Skoric Aleksandar Dimitrijevic Goran Cuturilo Petar Ivanovski

BACKGROUND Wiskott-Aldrich syndrome is a rare X-linked immunodeficiency disorder with a variable phenotype. CASE CHARACTERISTICS 3.5-year-old boy diagnosed with Wiskott-Aldrich syndrome. OBSERVATION Unusual and persistent thrombocytopenia with increased platelet volume (>10fL). He did not exhibit characteristic clinical and laboratory finding for the syndrome. OUTCOME Maternally inherited...

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