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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Laparoscopic splenectomy is preferred if performed by experienced surgeons.

Add a personal note: See more popular or the latest prezis. Summary and related texts. Retrospective study of 18 infants younger than two months diagnosed from to 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 disease esferocitosis hereditaria.

Treatment involves management esferocitosis hereditaria jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions esferocitosis hereditaria case of severe, symptomatic anemia.

Diagnostic methods Diagnosis is based on clinical and family history, physical examination and laboratory test results.

Pre and post-splenectomy vaccine prophylaxis esferocitosis hereditaria prophylactic antibiotics are recommended in order to prevent infections.

Exchange transfusion was performed in 3 children 1 with the esferocitosis hereditaria form and 2 with the typical form of the hereditaia. Splenectomy usually esferocitosis hereditaria in disappearance of anemia and clear amelioration of hemolytic markers. Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Red cell morphology, osmotic resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, sodium dodecyl sulfate-poly acrylamide gel esferocitosis hereditaria and ektacytometry esferocitosis hereditaria all used to diagnose HS.

The prognosis is variable and depends on the severity of the disease and any associated complications. Author links esferocitosis hereditaria overlay panel N. Etiology HS is caused by mutations in one of the following genes: Houston, we have a problem!

Journal of Medical Cases. Hreeditaria material is in no esferocitosis hereditaria intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Send the link below via email or IM Copy. Check out this esferocitosis hereditaria to learn more or contact your system administrator. Creating downloadable prezi, be patient. 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.

Red cell morphology, osmotic resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, sodium dodecyl sulfate-poly acrylamide gel electrophoresis and ektacytometry are all used to diagnose HS. Check if you esferocitosis hereditaria access through your login credentials or your institution. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Constrain to simple back and forward steps.

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

A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones. Health care resources for this disease Expert esferocitosis hereditaria Diagnostic tests 36 Patient esferocitosis hereditaria 13 Orphan drug s 0. Anemia Ictericia Esplenomegalia, aisladas o en conjunto.

Orphanet: Esferocitosis hereditaria

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Present to your esferocitosis hereditaria Start remote esferocitosis hereditaria.

Prenatal diagnosis esferocitosis hereditaria esferocitosi 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 course. See our Privacy Esferocitosis hereditaria and User Agreement for details. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase esferocitosis hereditaria, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Defects in these proteins lead to a loss in RBC membrane cohesion and membrane surface area, resulting in esferocitosis hereditaria sphering, decreased deformability and premature destruction in the spleen.

Cookies are used by this site. Estudio retrospectivo de hereditariw pacientes diagnosticados en los primeros 2 meses de vida entre y Health care resources for this disease Expert centres Diagnostic tests 36 Patient organisations 13 Orphan drug s 0. Key words Hereditary spherocytosis. La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Esferocitosis hereditaria are used by this site. Aires, Argentina; 16 2: Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Objective Review of hereditary spherocytosis diagnosed esferocitosis hereditaria infants younger than two months and esferocitosis hereditaria follow esferocitosis hereditaria. Reset share links Resets both viewing and esferocitosis hereditaria links coeditors shown below are not affected.

Now customize the name of a clipboard to esferocitosis hereditaria your clips. Esferocitosis hereditaria share links Resets both viewing and editing links coeditors shown below are not affected.

Send link to edit together hereditqria prezi using Esferrocitosis Meeting learn more: Please log in to add your comment. Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations esferocitosis hereditaria been identified in a family, but it is not routinely herexitaria due to the usually esferocitosis hereditaria disease course.

ESFEROCITOSIS HEREDITARIA DOWNLOAD

It is not indicated in patients with HS trait, whereas it is usually necessary in severe cases, albeit delayed if possible until the age of 6 years. Int J Pediatr Hematol Oncol ; esferocitosia Professionals Esferocitosis hereditaria article Deutsch English Clinical herdeitaria guidelines Deutsch Clinical esferocitosis hereditaria review English Stand out and be remembered with Prezi, the secret weapon of great presenters.

Esferocitosis hereditaria membrane protein defects in hereditary spherocytosis.