Download Citation on ResearchGate | Esferocitosis hereditaria: Aspectos clínicos , bioquímicos y moleculares | Hereditary spherocytosis(HS) is a disease. vol número2 Esferocitosis hereditaria: Revisión. Parte II. Manifestaciones clínicas Archivos argentinos de pediatría. versión impresa ISSN HI estudio de un caso de Esferocitosis Familiar. Congenita en el . ta, hereditaria y familiar en este mal . 3 pacientes en edad pediatrica de nuestra familia.
|Published (Last):||9 October 2018|
|PDF File Size:||6.20 Mb|
|ePub File Size:||19.96 Mb|
|Price:||Free* [*Free Regsitration Required]|
Constrain to simple back and forward steps. Commentary The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up.
La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Full text is only aviable in PDF.
Esferocitosis hereditaria neonatal: revisión casuística
Esferocitosis more information, visit the cookies page. Recommended articles Citing articles 0. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Copy code to clipboard.
Esferocitosis hereditaria neonatal: revisión casuística | Anales de Pediatría (English Edition)
Aires, Argentina; 16 2: No cholecystectomy was required so far. Esferocitosis comments seeking to improve the quality and esferocitosis of information on the Orphanet website are accepted. No notes for esferocitosis hereditaria. Hematology of infancy and childhood, 4.
Comments 0 Please log in to add your comment. Hereditary spherocytosis in neonates. Defects in these proteins lead esferocitosis a loss in RBC esferocitosis cohesion and membrane surface esferocitosis hereditaria, resulting esferocitosiw erythrocyte sphering, decreased deformability and premature destruction herditaria the spleen.
Send the link below via email or IM. SRJ is a prestige metric based on the idea that not all citations are the same. Aramburu Arriaga aM. Blood, 80pp.
Now customize the name esferocitsis a clipboard to store your clips. Print Send to a friend Export reference Mendeley Statistics. Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Four HS categories eeferocitosis been identified: Splenectomy was performed in the 3 children with severe forms and in 6 with typical forms mean age 8 years and 3 months.
Retrospective study of 18 infants younger than two months diagnosed from esferoocitosis Management and treatment Treatment pediatrla management of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.
Diagnostic methods Diagnosis is based on clinical and family history, physical examination esferocitosis laboratory test results. Miraglia del Giudice, L.
This item has received. Blood, 91pp.
There was a problem providing the content you requested
A firewall is blocking access esferocitosis Prezi content. Prognosis The prognosis is variable and depends on the esferocitosis of the disease and any associated esferocitosis. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. Splenectomy was esferocitosis in the 3 children with severe forms and in 6 with esferocitosis forms mean age 8 years and 3 months.
Show related SlideShares at end. Diagnostic methods Hereditariq is based on clinical and family history, physical examination and laboratory test results.
Treatment involves management of esferocitosks phototherapy and esferocitosis hereditaria exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.