نتایج جستجو برای: amegakaryocytic thrombocytopenia

تعداد نتایج: 24775  

Journal: :Hematology. American Society of Hematology. Education Program 2005
Blanche P Alter

Aplastic anemia may be inherited or acquired. The distinction between these lies not in the age of the patient, but in the clinical and laboratory diagnoses. Adult hematologists must consider adult presentations of the inherited disorders, in order to avoid incorrect management of their patients. Physicians for adult patients must also realize that children with inherited disorders now survive ...

Journal: :Blood 2005
Tetsuro Orita Hiroyuki Tsunoda Naohiro Yabuta Kiyotaka Nakano Takeshi Yoshino Yuichi Hirata Toshihiko Ohtomo Jun-Ichi Nezu Hirofumi Sakumoto Kouichiro Ono Mikiyoshi Saito Eiji Kumagai Masahiko Nanami Akihisa Kaneko Takashi Yoshikubo Masayuki Tsuchiya

Antibodies have brought valuable therapeutics in the clinical treatment of various diseases without serious adverse effects through their intrinsic features such as specific binding to the target antigen with high affinity, clinical safety as serum proteins, and long half-life. Agonist antibodies, furthermore, could be expected to maximize the value of therapeutic antibodies. Indeed, several Ig...

Journal: :Blood cells, molecules & diseases 2011
Chaim Jalas Sylvia L Anderson Tova Laufer Kristina Martimucci Alex Bulanov Xie Xie Josef Ekstein Berish Y Rubin

Congenital amegakaryocytic thrombocytopenia (MIM #604498) (CAMT) is a rare inherited disease presenting as severe thrombocytopenia in infancy. Untreated, many CAMT patients develop aplastic anemia within the first decade of life; the only effective treatment of CAMT is bone marrow transplantation. CAMT is the result of the presence of homozygous or compound heterozygous mutations in the thrombo...

2014
Gabrielle Elena Brown Hani M. Babiker Carlos L. Cantu Andrew M. Yeager Ravitharan Krishnadasan

Acquired amegakaryocytic thrombocytopenia (AAT) is a rare hematological disorder causing severe thrombocytopenia and bleeding. Previous in vitro studies postulated both cell-mediated suppression of megakaryocytopoiesis in early megakaryocytic progenitor cells and humoral-mediated suppression by anti-thrombopoietin antibodies as possible etiologies of AAT. Patients with AAT usually present with ...

Journal: :Haematologica 2010
Hannah Tamary Daniella Nishri Joanne Yacobovich Rama Zilber Orly Dgany Tanya Krasnov Shraga Aviner Polina Stepensky Shoshana Ravel-Vilk Menachem Bitan Chaim Kaplinsky Ayelet Ben Barak Ronit Elhasid Joseph Kapelusnik Ariel Koren Carina Levin Dina Attias Ruth Laor Isaac Yaniv Philip S Rosenberg Blanche P Alter

BACKGROUND Inherited bone marrow failure syndromes are rare genetic disorders characterized by bone marrow failure, congenital anomalies, and cancer predisposition. Available single disease registries provide reliable information regarding natural history, efficacy and side effects of treatments, and contribute to the discovery of the causative genes. However, these registries could not shed li...

2017
Shojiro Ichimata Mikiko Kobayashi Kohei Honda Soichiro Shibata Akihiro Matsumoto Hiroyuki Kanno

We report the first case of a patient with hepatitis C virus (HCV) infection and idiopathic thrombocytopenic purpura (ITP), who later developed acquired amegakaryocytic thrombocytopenia (AAMT), with autoantibodies to the thrombopoietin (TPO) receptor (c-Mpl). A 64-year-old woman, with chronic hepatitis C, developed severe thrombocytopenia and was diagnosed with ITP. She died of liver failure. A...

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