نتایج جستجو برای: g6pc3

تعداد نتایج: 42  

2013
Siddharth Banka William G Newman

The G6PC3 gene encodes the ubiquitously expressed glucose-6-phosphatase enzyme (G-6-Pase β or G-6-Pase 3 or G6PC3). Bi-allelic G6PC3 mutations cause a multi-system autosomal recessive disorder of G6PC3 deficiency (also called severe congenital neutropenia type 4, MIM 612541). To date, at least 57 patients with G6PC3 deficiency have been described in the literature.G6PC3 deficiency is characteri...

2010
Hyun Sik Jun Young Mok Lee Yuk Yin Cheung David H. McDermott Philip M. Murphy Suk See De Ravin Brian C. Mansfield Janice Y. Chou

G6PC3 deficiency, characterized by neutropenia and neutrophil dysfunction, is caused by deficiencies in the endoplasmic reticulum (ER) enzyme glucose-6-phosphatase(G6Paseor G6PC3) that converts glucose6-phosphate (G6P) into glucose, the primary energy source of neutrophils. Enhanced neutrophil ER stress and apoptosis underlie neutropenia in G6PC3 deficiency, but the exact functional role of G6P...

Journal: :Iranian journal of allergy, asthma, and immunology 2011
Zahra Alizadeh Mohammad Reza Fazlollahi Payman Eshghi Amir Ali Hamidieh Mohsen Ghadami Zahra Pourpak

Severe congenital neutropenia (SCN) is a rare primary immunodeficiency. Different genes are found to be associated with SCN, including ELA2, HAX1, WAS, GFI1, G-CSFR. Also, recently G6PC3 as a rare gene in SCN has been reported. Patients with G6PC3 often have cardiac and/or urogenital malformations. Two patients with persistent severe neutropenia, recurrent infections and maturation arrest at pr...

Journal: :Blood 2012
Hyun Sik Jun Yuk Yin Cheung Young Mok Lee Brian C Mansfield Janice Y Chou

Glucose-6-phosphatase-β (G6Pase-β or G6PC3) deficiency, also known as severe congenital neutropenia syndrome 4, is characterized not only by neutropenia but also by impaired neutrophil energy homeostasis and functionality. We now show the syndrome is also associated with macrophage dysfunction, with murine G6pc3(-/-) macrophages having impairments in their respiratory burst, chemotaxis, calcium...

Journal: :Haematologica 2010
Manuela Germeshausen Cornelia Zeidler Manfred Stuhrmann Marina Lanciotti Matthias Ballmaier Karl Welte

Severe congenital neutropenia a clinically and genetically heterogeneous disorder. Mutations in different genes have been described as causative for severe neutropenia, e.g. ELANE, HAX1 and G6PC3. Although congenital neutropenia is considered to be a group of monogenic disorders, the phenotypic heterogeneity even within the yet defined genetic subtypes points to additional genetic and/or epigen...

Journal: :Glycobiology 2011
Bu'hussain Hayee Aristotelis Antonopoulos Emma J Murphy Farooq Z Rahman Gavin Sewell Bradley N Smith Sara McCartney Mark Furman Georgina Hall Stuart L Bloom Stuart M Haslam Howard R Morris Kaan Boztug Christoph Klein Bryan Winchester Edgar Pick David C Linch Rosemary E Gale Andrew M Smith Anne Dell Anthony W Segal

Glucose-6-phosphatase, an enzyme localized in the endoplasmic reticulum (ER), catalyzes the hydrolysis of glucose-6-phosphate (G6P) to glucose and inorganic phosphate. In humans, there are three differentially expressed glucose-6-phosphatase catabolic genes (G6PC1-3). Recently, it has been shown that mutations in the G6PC3 gene result in a syndrome associating congenital neutropenia and various...

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
Claire Desplantes Marie Louise Fremond Blandine Beaupain Jean Luc Harousseau Agnès Buzyn Isabelle Pellier Gaelle Roques Pierre Morville Catherine Paillard Julie Bruneau Lucile Pinson Eric Jeziorski Jean Pierre Vannier Capucine Picard Florence Bellanger Norma Romero Loïc de Pontual Hélène Lapillonne Patrick Lutz Christine Bellanné Chantelot Jean Donadieu

BACKGROUND The purpose of this study was to describe the natural history of severe congenital neutropenia (SCN) in 14 patients with G6PC3 mutations and enrolled in the French SCN registry. METHODS Among 605 patients included in the French SCN registry, we identified 8 pedigrees that included 14 patients with autosomal recessive G6PC3 mutations. RESULTS Median age at the last visit was 22.4 ...

2011
Andrew R. Cullinane Thierry Vilboux Kevin O’Brien James A. Curry Dawn M. Maynard Hannah Carlson-Donohoe Carla Ciccone Thomas C. Markello Meral Gunay-Aygun Marjan Huizing William A. Gahl

We evaluated a 32-year-old woman whose oculocutaneous albinism (OCA), bleeding diathesis, neutropenia, and history of recurrent infections prompted consideration of the diagnosis of Hermansky-Pudlak syndrome type 2. This was ruled out because of the presence of platelet δ-granules and absence of AP3B1 mutations. As parental consanguinity suggested an autosomal recessive mode of inheritance, we ...

Journal: :Iranian journal of allergy, asthma, and immunology 2013
Zahra Alizadeh Mohammad Reza Fazlollahi Massoud Houshmand Marzieh Maddah Zahra Chavoshzadeh Amir Ali Hamidieh Bibi Shahin Shamsian Payman Eshghi Samaneh Bolandghamat Pour Hoda Sadaaie Jahromi Mahboobeh Mansouri Masoud Movahedi Mohsen Nayebpour Zahra Pourpak Mostafa Moin

Severe congenital neutropenia (SCN) is a rare primary immunodeficiency disease. Different genes are found to be associated with SCN, including ELA2, HAX1, WAS, GFI1, G-CSFR and G6PC3. The aim of this study was to find different gene mutations responsible for SCN in Iranian patients. Twenty-seven patients with SCN referred to Immunology, Asthma and Allergy Research Institute during a five year p...

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