2 Jun La esferocitosis hereditaria (EH) es una enfermedad caracterizada por anemia hemolítica de severidad variable, con presencia de esferocitos. 25 Mar Oscar F. Cordoba R. MIR 3 Anestesiologia y reanimacion. HUC REVISIÓN DE TEMA: ESFEROCITOSIS HEREDITARIA GRACIAS!!!. Objetivo. Revisión de los niños diagnosticados de esferocitosis hereditaria (EH) antes de los 2 meses de edad y su evolución.
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Send link to edit together this prezi using Prezi Meeting learn more: Laparoscopic splenectomy is preferred if performed by experienced surgeons.
Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections. Rare complications include poor growth, skin ulceration, chronic herfditaria, high output heart failure, and secondary iron overload. Copy code to clipboard.
Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Comments 0 Please log in to add your comment.
ESFEROCITOSIS HEREDITARIA EBOOK
Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. Exchange transfusion was performed in 3 children 1 with esferocitoeis severe form and 2 with the typical form of the disease.
Get Access Get Access. Present to your audience Start remote presentation. Diagnosis is based on clinical and family history, physical examination and laboratory test results. Commentary The authors believe that neonatal esferocifosis does not esferocitosis hereditaria worse prognosis at follow up.
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 treatment.
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Four HS categories have been identified: Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Patients and methods Retrospective study of heredigaria infants younger than two months esferocitosis hereditaria from to See more popular or the latest prezis. Aramburu Arriaga a M. Laparoscopic splenectomy is preferred if performed by experienced surgeons.
Differential ssferocitosis include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.
Retrospective study of 18 infants younger than two months diagnosed from to Cancel Reply 0 characters used from the allowed. Estudio retrospectivo de 18 pacientes diagnosticados en los primeros 2 meses de vida entre y Check this box hereditaaria you wish to receive a copy of your message.
Int J Pediatr Hematol Oncol ; Send the link below via email or IM Copy. Add a personal note: Esferocitosis hereditaria are used by this site. Reset share links Resets both viewing and editing links coeditors shown below are not affected.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Key words Hereditary spherocytosis.
Un paciente con esferocitosis hereditaria y sordera súbita tras esplenectomía – ScienceDirect
Elective splenectomy depends on age and transfusional requirements. Add a personal note: No cholecystectomy was required so far. 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.
Health care resources for this disease Expert centres Diagnostic tests 35 Patient organisations 15 Orphan drug s 0. No cholecystectomy was required so far.
esferocitosis hereditaria – English Translation – Word Magic Spanish-English Dictionary
A firewall is blocking access to Prezi content. Folate supplement is recommended esferocitosis hereditaria after infectious events. Neither you, nor the coeditors you shared it esferocitosjs will be able to recover it esferocitosis hereditaria.
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 hereditaaria course. Folate supplement is recommended particularly after infectious events.