نتایج جستجو برای: severe congenital neutropenia

تعداد نتایج: 443969  

Journal: :Blood 2000
M H Freedman M A Bonilla C Fier A A Bolyard D Scarlata L A Boxer S Brown B Cham G Kannourakis S E Kinsey P G Mori T Cottle K Welte D C Dale

Granulocyte colony-stimulating factor (G-CSF) has had a major impact on management of "severe chronic neutropenia," a collective term referring to congenital, idiopathic, or cyclic neutropenia. Almost all patients respond to G-CSF with increased neutrophils, reduced infections, and improved survival. Some responders with congenital neutropenia have developed myelodysplastic syndrome and acute m...

Journal: :Turk pediatri arsivi 2015
Tiraje Celkan Begüm Şirin Koç

Neutrophils have an important role in host defense and acute inflammation. It is well known that susceptibility to infection increases when the neutrophil count is low. Neutropenia were classified as mild, moderate and severe according to the neutrophil counts, or acute and chronic depending on the duration of neutropenia, or congenital and acquired according to the mechanism. The patients with...

Journal: :Molecular and cellular biology 2009
Stephen J Salipante Meghan E B Rojas Brice Korkmaz Zhijun Duan Jeremy Wechsler Kathleen F Benson Richard E Person H Leighton Grimes Marshall S Horwitz

"Neutropenia" refers to deficient numbers of neutrophils, the most abundant type of white blood cell. Two main forms of inherited neutropenia are cyclic neutropenia, in which neutrophil counts oscillate with a 21-day frequency, and severe congenital neutropenia, in which static neutropenia may evolve at times into leukemia. Mutations of ELA2, encoding the protease neutrophil elastase, can cause...

Journal: :The New England journal of medicine 1995
F Dong R K Brynes N Tidow K Welte B Löwenberg I P Touw

BACKGROUND In severe congenital neutropenia the maturation of myeloid progenitor cells is arrested. The myelodysplastic syndrome and acute myeloid leukemia develop in some patients with severe congenital neutropenia. Abnormalities in the signal-transduction pathways for granulocyte colony-stimulating factor (G-CSF) may play a part in the progression to acute myeloid leukemia. METHODS We isola...

Journal: :Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2014
Giulia Angelino Roberta Caruso Patrizia D'Argenio Francesca Ippolita Calò Carducci Roberto Pascone Marina Lanciotti Caterina Cancrini Paolo Palma Alessandro Aiuti Paolo Rossi Andrea Finocchi

BACKGROUND Neutropenia is not uncommon in childhood. The aim of our study was to analyze the underlying causes of neutropenia and to evaluate its clinical significance in a series of children referred to our center. METHODS One hundred and four consecutive children with neutropenia were enrolled in this study. Clinical and laboratory features were analyzed. RESULTS The majority of patients ...

Journal: :Iranian journal of allergy, asthma, and immunology 2012
Tahmineh Salehi Mohammad Reza Fazlollahi Marzieh Maddah Mohsen Nayebpour Mojtaba Tabatabaei Yazdi Zahra Alizadeh Peyman Eshghi Zahra Chavoshzadeh Masoud Movahedi Amir Ali Hamidieh Taher Cheraghi Zahra Pourpak Mostafa Moin

Severe congenital neutropenia is one of primary immunodeficiency disorders that characterized by severe neutropenia and is associated with severe systemic bacterial infections from early infancy. Granulocyte colony stimulating factor (GCSF) is clinically used as a treatment for congenital and acquired neutropenia. The aim of this study was evaluation of GCSF (PD- Grastim) in treatment of these ...

Journal: :Journal of investigational allergology & clinical immunology 2008
A Fahimzad Z Chavoshzadeh H Abdollahpour C Klein N Rezaei

Severe congenital neutropenia (SCN) is a primary immunodeficiency disease characterized by early onset of severe bacterial infection and persistent severe neutropenia. We describe an SCN patient with a history of recurrent infections. The clinical course was complicated by necrosis of the nasal cartilage due to mucormycosis. Molecular studies revealed a homozygous germline HAX1 mutation. Fungal...

2014
Lucia Dora Notarangelo Gianfranco Savoldi Sara Cavagnini Veronica Bennato Sabrina Vasile Alba Pilotta Alessandro Plebani Fulvio Porta

Severe Congenital Neutropenia type 4 (SCN4, OMIM 612541) is a rare autosomal recessive disease due to mutations in the G6PC3 gene. The phenotype comprises neutropenia of variable severity and other anomalies including congenital heart defects, prominent superficial veins, uro-genital anomalies, facial dysmorphism, growth and developmental delay and intermittent thrombocytopenia. In some patient...

2014
Hye-Kyung Cho In Sang Jeon

Severe congenital neutropenia (SCN) is a heterogeneous group of disorders with a defect in granulopoiesis causing marked neutropenia and severe bacterial infections. A 17-month-old girl (patient 1) was admitted due to cervical lymphadenitis caused by methicillin-resistant Staphylococcus aureus, with neutropenia. She had Pseudomonas aeruginosa sepsis and peritonitis with perforated appendicitis ...

Journal: :Blood 2008
Nancy Berliner

Severe congenital neutropenia (SCN) was first described just over 50 years ago. The progress in elucidating the clinical features and molecular pathophysiology of SCN closely parallels the progressive growth in our understanding of myelopoiesis. In this historical review, I have delineated this parallel progression in our understanding of the processes of granulocyte differentiation and the pat...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید