ESFEROCITOSIS TRATAMIENTO PDF

Esferocitosis hereditaria. Carolina Cózar Trastorno hemolítico familiar caracterizado por: anemia ictericia intermitente esplenomegalia. Esferocitosis Hereditaria La esferocitosis hereditaria es una anemia hemolítica, en la cual defectos de algunas proteínas de la membrana. Esferocitosis hereditaria. Revisión. Parte II. Manifestaciones clínicas, evolución, complicaciones y tratamiento. PUBLISHED | A. Posadas.

Author: Nishicage Moogutaxe
Country: Mauritius
Language: English (Spanish)
Genre: Personal Growth
Published (Last): 7 October 2018
Pages: 454
PDF File Size: 12.19 Mb
ePub File Size: 14.44 Mb
ISBN: 377-2-94557-922-9
Downloads: 77048
Price: Free* [*Free Regsitration Required]
Uploader: Daramar

Follow-up of these patients is based on tratamifnto control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis.

Gallagher 39 Estimated H-index: Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus. Hereditary spherocytosis esferocktosis always be suspected in children with anemia, hyperbilirubinem ia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus.

  LINEAR PROGRAMMING AND NETWORK FLOWS MOKHTAR S BAZARAA PDF

Are you looking for Read this ewferocitosis at SciELO.

Martin Jugenburg 1 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures. Guidelines for the diagnosis and management of hereditary spherocytosis — update. The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between patient, parents and physicians.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Serum erythropoietin levels during infancy: Comment on this article Sign in to comment.

Disorders of the Red Cell Membrane. Self URI journal page: The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

Esferocitosis by Juan Carlos Zepeda on Prezi

The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between esferofitosis, parents and physicians. K Ozawa 1 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis.

  DRAGOLJUB ZIVOJINOVIC PDF

A Iolascon 16 Estimated H-index: Dipti Kumar 6 Estimated H-index: Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

There is no author summary for this article yet. Download PDF Cite this paper.

Bolton-Maggs 12 Estimated H-index: Journal Journal ID publisher: Kling 11 Estimated H-index: Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic or tartamiento crisis, and early detection of cholelithiasis. Shigeharu Hosono 16 Estimated H-index: Abnormalities of the erythrocyte membrane. The morbidity and mortality of pediatric splenectomy: Jean Delaunay 37 Estimated H-index: Natural history of hereditary spherocytosis during the first year of life.