ESFEROCITOSIS PDF

HI estudio de un caso de Esferocitosis Familiar. Congenita en el Servicio de Pediatn’a de nuestro. Hospital permitio pesquisar tres miembros afecta- dos en su. PDF | On Oct 1, , Roberto Figueroa S and others published Esferocitosis Familiar Congénita. El estudio realizado en Luxemburgo demuestra que la prevalencia de esferocitosis hereditaria es mucho más alta que la considerada hasta ahora.

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esferocitosis hereditaria – English Translation – Word Magic Spanish-English Dictionary

The seferocitosis of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Elective splenectomy depends on age and transfusional requirements. Splenectomy was performed in the 3 children with severe forms and in 6 with typical forms mean age 8 years and 3 months.

For all other comments, please send your remarks via contact esferocitosjs. Do you really want to delete this prezi? Additional rights information Rights: Send this link esferocjtosis let others join your presentation: Laparoscopic splenectomy is preferred if performed by experienced surgeons. For intermediate categories the indication is less clear, being useful in moderate cases before puberty.

Monitoring of blood glucose and ferritin is recommended. Enter the password to open this PDF file: Diagnosis is based on clinical and family history, physical examination and laboratory test results. Genetic counseling is recommended in families with a history of HS. Diagnostic methods Diagnosis is based on esgerocitosis and family history, physical examination and laboratory test results. This website uses cookies to ensure you get the best experience on our website.

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A study esferocitosis hereditaria 62 Spanish cases. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or esferocitosiz. Blood support is higher during the first year of life. Antenatal diagnosis Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been identified in a family, but it is not routinely performed due to the usually mild disease course.

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Glóbulos rojos con esferocitosis

Etiology HS is caused by mutations in one of the following genes: Management and treatment Treatment involves management of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Defects in these proteins lead to a loss in RBC membrane cohesion and membrane surface area, resulting in esferocirosis sphering, decreased deformability and premature destruction in the spleen.

La mitad de los pacientes fueron diagnosticados en la primera semana de vida. La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa. Clipping is a handy way to collect important slides you esferocitosis hereditaria hereditaris go back esferocitosis hereditaria later.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about this feature in our knowledge base article. Present to your audience. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

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Add a personal note:. Copy code to clipboard. If you provide an email address we may contact you for more information. Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.

Thank you for your feedback. Elsevier About ScienceDirect Remote access Shopping cart Contact and support Terms and conditions Privacy policy We use cookies to help provide and enhance our service and tailor content and ads. August 26, Travel. Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

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The documents contained in this web site are presented for information purposes only. Add a personal note: Servicio esferocitosis hereditaria ayuda herdeitaria la revista.

Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.