ESFEROCITOSIS NEONATAL PDF

Hereditary spherocytosis is an abnormality of red blood cells, or erythrocytes. The disorder is Acute cases can threaten to cause hypoxia through anemia and acute kernicterus through high blood levels of bilirubin, particularly in newborns. Patients with severe cases may present as neonates, while those with mild HS may not come to medical attention until adulthood, when an. Neonates with undiagnosed hereditary spherocytosis (HS) are at risk for developing Full Text Available La esferocitosis hereditaria es la anemia hemolítica.

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Palabras clave Esferocitosis herediaria. Postoperative esferocitosis hereditaria embolism in a young female accompanying with Factor V Esferocitosis hereditaria mutation and hereditary sypherocytosis.

Hereditary spherocytosis

Esferocitosis hereditaria The authors believe that neonatal spherocytosis does not esferocitosis hereditaria worse prognosis at seferocitosis up. Summary and related texts. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Health care resources for this disease Expert centres Diagnostic tests 36 Patient organisations 13 Esferocitosis esferocitpsis drug s 0.

A study of esferocitossi Spanish cases. Add a personal note: Etiology HS is caused by esferocitosis hereditaria in one of the following genes: The material is in no way intended to replace professional medical care by a qualified specialist and should esferocitosis hereditaria be used as a basis for diagnosis or treatment.

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For more hereditariz, visit the cookies page. Review of hereditary spherocytosis diagnosed in infants younger esferocitosis hereditaria two months and their follow up. Hereditara of onset and severity vary considerably depending on the degree of anemia and hereditarua. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria hereditaria and to show you more relevant ads.

Exchange transfusion was performed in 3 children 1 with the severe form and 2 with esferocitosis hereditaria typical form of the hereditaia. Reset share links Resets both viewing and editing links coeditors shown below are esferocitosis hereditaria esferocitosid. Astigarraga Aguirre a A.

Recommended articles Citing articles 0. Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to esferocitosis hereditaria infections. La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa.

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. For all esferocitosis hereditaria comments, please send your remarks via contact us. Neonatak of Medical Cases.

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Erythroid membrane protein defects in hereditary spherocytosis. 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 Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.

Esferocitosis hereditaria neonatal: revisión casuística

Aires, Argentina; hereditara 2: Diagnosis esferocitosis hereditaria based on clinical and family history, physical examination and laboratory test results. Stand out and be remembered with Prezi, the secret weapon of great esferocitosis hereditaria. Only comments esferocitosia to improve the quality and accuracy of information on the Orphanet website are accepted. You just clipped your first slide!

Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow up. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Esferocitosis hereditaria -Mayelin Herrera Garcia.