نتایج جستجو برای: platelet disorder

تعداد نتایج: 699157  

Journal: :Progress in neuro-psychopharmacology & biological psychiatry 2008
Zrnka Kovacic Neven Henigsberg Nela Pivac Gordana Nedic Andrea Borovecki

Posttraumatic stress disorder (PTSD) is a serious and global problem, a psychiatric disorder that frequently occurs with different comorbidities, and is associated with a high suicide rate. Pathophysiologically, both PTSD and suicidal behavior are related to disturbances in the central serotonergic system. Serotonin (5-hydroxytryptamine, 5-HT) controls emotional behavior, anxiety, impulsivity a...

Journal: :Blood 2001
W H Kahr S Zheng P M Sheth M Pai A Cowie M Bouchard T J Podor G E Rivard C P Hayward

The Quebec platelet disorder (QPD) is an autosomal dominant platelet disorder associated with delayed bleeding and alpha-granule protein degradation. The degradation of alpha-granule, but not plasma, fibrinogen in patients with the QPD led to the investigation of their platelets for a protease defect. Unlike normal platelets, QPD platelets contained large amounts of fibrinolytic serine protease...

Journal: :international journal of pediatrics 0
kamleshun ramphul department of pediatrics, shanghai xin hua hospital affiliated to the shanghai jiao tong university school of medicine, china. sunjaye ramjuttun department of pediatrics, sir seewoosagur ramgoolam national hospital, mauritius, china. vinita poorun department of pediatrics, sir seewoosagur ramgoolam national hospital, mauritius, china.

wiskott-aldrich is an x-lined recessive disorder typically characterized by thrombocytopenia, eczema and recurrent infections. we report the four year treatment progress of a six year old boy who initially presented with vesicular lesions over the trunk, upper and lower extremities and face and blood tinged stools at the age of 2 weeks. from the family pedigree, there were two suspected cases t...

2014
Amira Abdel Moneam Adly

Immune thrombocytopenic purpura (ITP) is a common autoimmune disorder resulting in isolated thrombocytopenia. It is a bleeding disorder characterized by low platelet counts due to decreased platelet production as well as increased platelet destruction by autoimmune mechanisms. ITP can present either alone (primary) or in the setting of other conditions (secondary) such as infections or altered ...

Journal: :Psychosomatic medicine 2005
Erica C Bruce Dominique L Musselman

Platelets, the smallest corpuscular component of human blood, are central to various crucial biologic pathways in the human body. Diminished platelet function is thought to contribute to the increased risk of ischemic heart disease in patients with major depressive disorder, and to the increased morbidity and diminished survival of depressed patients after an index myocardial infarction. We rev...

2018
Yasuhiro Watanabe Naomi Shimizu Masahiro Iwakawa Takashi Yamaguchi Noriko Ban Hidetoshi Kawana Atsuhito Saiki Emiko Sakaida Chiaki Nakaseko Yasuhiro Matsuura Nobuyuki Aotsuka Hideaki Bujo Ichiro Tatsuno

Osteogenesis imperfecta (OI) is a rare inherited disorder of the connective tissue with many reports on its association with bleeding diatheses. OI patients with blue sclera, hearing loss, and bone vulnerability are classified as having van der Hoeve syndrome. Here, we report the first case of rapidly progressing, massive esophageal submucosal hematoma in this syndrome. Bleeding in OI is report...

2012
Lalitha Nayak Alvin H. Schmaier

The antiestrogenic drug tamoxifen, used in patients with breast cancer, is associated with an increase in arterial and venous thrombotic events, the mechanism of which is not clearly understood. We report a case of a lady who presented with new bruising and prolonged bleeding following a tooth extraction 4-6 weeks after starting tamoxifen. Investigations were consistent with an acquired platele...

2016
Xin-guang Liu Ming Hou

Primary immune thrombocytopenia (ITP) is a complex autoimmune disorder in which the patient's immune system reacts with platelet autoantigens resulting in immune-mediated platelet destruction and/or suppression of platelet production. Corticosteroids can induce sustained remission rates in 50% to 75% of patients with active ITP. For these patients who are unresponsive to glucocorticoids, or rel...

2012
Anselm Chi-wai Lee

An 11-year-old American boy was staying with his family in Indonesia. He presented with a 5-month history of recurrent bruises and ecchymosis. A clinical diagnosis of acquired platelet dysfunction with eosinophilia was made when his full blood counts showed hypereosinophilia (7.4×10(9)/L) with normal platelet count and gray platelets under the microscope. The diagnosis was supported by abnormal...

Journal: :Kathmandu University medical journal 2012
M R Sigdel D S Shah M P Kafle K B Raut

Immune thrombocytopenic purpura (ITP) is a hematological disorder characterized by immunologically mediated destruction of platelets and absence of other causes of thrombocytopenia. Treatment is required when the low platelet count entails risk of serious bleeding. Steroid is the first line of management. Acute refractory ITP with very low platelet count is variably treated with high dose stero...

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