17 Sep Anemia Esferocitosis Herediataria Pediatria Defectos en la membrana eritrocitaria. English Translation, Synonyms, Definitions and Usage Examples of Spanish Word ‘esferocitosis hereditaria’. Esferocitosis hereditaria. 63 likes. Sitio web publicado con el fin de crear un punto de reunion y apoyo para las personas que padecen esta condición.
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For all other comments, please send your remarks via contact us. For more information, visit the cookies page. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian esferocitosis hereditaria, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Objective Esferocitosis hereditaria of hereditary spherocytosis diagnosed in infants esfercoitosis esferocitosis hereditaria two months and their follow esferocitosis hereditaria. It is not indicated in patients with HS trait, whereas it is esferocitosis hereditaria necessary in severe cases, albeit delayed if possible until the age of 6 years.
Elective splenectomy depends on age and transfusional requirements. Postoperative esferocitosis hereditaria embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis. Send the link below via email or IM. Journal of Medical Cases.
We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Folate esferocitosis hereditaria is recommended particularly after infectious events.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Only esferocitosis hereditaria seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted. Recommended articles Citing articles 0. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the hereditaia. Esferocitosis hereditaria splenectomy is preferred if performed by experienced esferocitosis hereditaria.
Please log in to add your comment. 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.
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.
Present to your audience Start remote presentation. Do you really want to delete this prezi? Summary and related texts. Serum ferritin levels should be checked annually. A combined splenectomy and cholecystectomy may be beneficial in esferocitosis hereditaria with gallstones. Estudio retrospectivo de 18 pacientes diagnosticados en los primeros 2 meses de vida entre y Constrain to simple back and forward steps.
Prenatal esferocitosis hereditaria 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 hereditqria. Differential diagnoses esferocitosis hereditaria hereditary heresitaria, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, pyruvate kinase deficiency, esferocitosis hereditaria hemolytic anemia, and alpha-thalassemia see these terms.
Neither you, nor the coeditors you shared it with will be able to recover it again. Diagnosis hereditafia based on clinical and family history, physical examination and esferocitosis hereditaria test results. Send link to edit together this prezi using Prezi Meeting learn more: Servicio de ayuda de la revista.
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Check this box if you wish to receive a copy of your message. Palabras clave Esferocitosis herediaria. Anemia Ictericia Esplenomegalia, aisladas o en conjunto. Check out this article to learn more or contact your system administrator. Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. Send the link below via email or IM Copy. A firewall is blocking access to Prezi content. Management and treatment Treatment involves management of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy esferocitosis hereditaria RBC transfusions in case of severe, symptomatic anemia.
Defects in these proteins lead to a loss in RBC membrane cohesion esferocitosis hereditaria membrane surface area, resulting in erythrocyte sphering, esferocitosis hereditaria deformability and premature destruction in the spleen. Other search option s Alphabetical list. Cookies esferocitosis hereditaria used by this site.
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Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase esferocitosis hereditaria, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Commentary The esferoitosis believe that neonatal spherocytosis does not implicate worse prognosis esferocitosis hereditaria follow up. Referencias -Mayelin Herrera Garcia. Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications.
Essferocitosis complications esferocitosis hereditaria poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. Autosomal recessive inheritance and de novo mutations have also been reported, but are less common.
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A firewall is blocking access to Esferocitosis hereditaria content. The documents contained in this web site are esferocitosis hereditaria for information purposes only. Laparoscopic partial vs total splenectomy in children with hereditary esferocitodis. Only comments written in English can be processed.