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1.
Transfus Clin Biol ; 17(3): 138-42, 2010 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-20655264

RESUMEN

Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in one or more of the proteins composing red blood cell membrane. As a result, red blood cells have an abnormal shape, higher metabolic requirements, and are prematurely trapped and destroyed in the spleen. Hereditary spherocytosis, including the very mild or subclinical forms, is the most common cause of non-immune hemolytic anemia among people of Northern European ancestry, with a prevalence of approximately 1 in 2000. However very mild forms of the disease may be much more common. Hereditary spherocytosis is inherited in a dominant fashion in 75% of cases, whereas the remaining are truly recessive cases and de novo mutations. This review reports current concepts on red cell membrane structure and it will attempt to clarify molecular defects leading to spherocyte and their consequences.


Asunto(s)
Esferocitosis Hereditaria/sangre , Anemia Hemolítica/epidemiología , Anemia Hemolítica/genética , Proteína 1 de Intercambio de Anión de Eritrocito/genética , Diagnóstico Diferencial , Deformación Eritrocítica/genética , Membrana Eritrocítica/metabolismo , Europa (Continente)/epidemiología , Genes Dominantes , Genes Recesivos , Humanos , Proteínas de la Membrana/sangre , Proteínas de la Membrana/genética , Mutación , Esferocitosis Hereditaria/diagnóstico , Esferocitosis Hereditaria/genética , Esferocitosis Hereditaria/metabolismo , Población Blanca/genética
2.
J Pediatr ; 152(1): 136-9, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18154916

RESUMEN

DMT1 deficiency causes microcytic hypochromic anemia due to decreased erythroid iron utilization. Anemia is present from birth. Transferrin saturation is high and serum ferritin is mildly elevated, despite liver iron overload. DMT1 deficiency must be considered in the differential diagnosis of microcytic hypochromic anemia observed in the newborn period.


Asunto(s)
Anemia Hipocrómica/genética , Proteínas de Transporte de Catión/genética , Genes Recesivos , Mutación , Anemia Hipocrómica/diagnóstico , Anemia Hipocrómica/tratamiento farmacológico , Proteínas de Transporte de Catión/deficiencia , Diagnóstico Diferencial , Eritrocitos/metabolismo , Eritropoyetina/uso terapéutico , Ferritinas/sangre , Genotipo , Humanos , Recién Nacido , Quelantes del Hierro/uso terapéutico , Fenotipo , Transferrina/metabolismo
3.
Surg Oncol ; 16 Suppl 1: S121-4, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18032026

RESUMEN

Postoperative infectious complications still represent a relevant problem in colorectal surgery. They always results in suffering for the patients and often prolonged hospitalization. Furthermore, they result in additional expenses to cover the cost of antibiotics, blood derivates, total parenteral nutrition, nursing and additional surgical procedures. Prevention and control of hospital infections start with surveillance, which is an important means to constantly evaluate the local bacterial epidemiology. An infection surveillance program finalized to minimize the incidence of postoperative infections through the respect of available techniques leads to a better quality of work in each surgical unit, to a decrease in postoperative hospital stay and to cost reduction.


Asunto(s)
Colon/cirugía , Recto/cirugía , Infección de la Herida Quirúrgica/prevención & control , Profilaxis Antibiótica , Proteína C-Reactiva/metabolismo , Humanos , Interleucina-6/metabolismo , Laparoscopía , Neutrófilos/metabolismo , Factores de Riesgo , Infección de la Herida Quirúrgica/etiología , Linfocitos T/metabolismo
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