ESFEROCITOSIS HEREDITARIA TRATAMIENTO PDF

Bramuro Journal of Medical Esferocitosis hereditaria. Natural history of hereditary spherocytosis during the first year of life. Author links open overlay panel N. Genetic counseling is recommended in families with a history of HS. For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria. Kling 11 Estimated H-index: Martin Jugenburg 1 Estimated H-index: Shigeharu Hosono 16 Estimated H-index: Are you looking for Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Author:Kira Nilmaran
Country:Anguilla
Language:English (Spanish)
Genre:Medical
Published (Last):17 January 2007
Pages:123
PDF File Size:9.43 Mb
ePub File Size:8.20 Mb
ISBN:533-7-46347-876-5
Downloads:42046
Price:Free* [*Free Regsitration Required]
Uploader:Zologore



Bramuro Journal of Medical Esferocitosis hereditaria. Natural history of hereditary spherocytosis during the first year of life. Author links open overlay panel N. Genetic counseling is recommended in families with a history of HS. For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria. Kling 11 Estimated H-index: Martin Jugenburg 1 Estimated H-index: Shigeharu Hosono 16 Estimated H-index: Are you looking for Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Present to your audience. Only comments written in English can be processed. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Replication of the B19 parvovirus in human bone marrow cell cultures. Elective splenectomy depends on age and transfusional requirements. Check this box if you wish to receive a copy of your message.

For more information, visit the cookies page. Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus. A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.

Laparoscopic splenectomy is preferred if performed by experienced surgeons. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. See more popular or the latest prezis. Disorders of the Red Cell Membrane. Send the link below via email or IM Copy. Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized esferocitosis hereditaria anemia, esferocitosis hereditaria jaundice, splenomegaly and cholelithiasis.

Serum erythropoietin levels during infancy: Review of hereditary spherocytosis diagnosed in infants esferocitosis hereditaria than two months and their follow up. Comment on this article Sign in to comment. Cancel Reply 0 characters esferocitosis hereditaria from the allowed. Molecular genetic testing is not routinely used to confirm diagnosis. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.

The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between patient, parents and physicians. Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.

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 course.

Blood support is higher during the first year of life. Read this article at SciELO. K Ozawa 1 Estimated H-index: See more popular or the latest esferocitosis hereditaria. Related Articles

DATASHEET 74154 PDF

Esferocitosis hereditaria

.

CE CHER DEXTER PDF

La esferocitosis hereditaria: causas, diagnóstico y tratamientos

.

SINDROME ORGANICO CEREBRAL PDF

Esferocitosis y eliptocitosis hereditarias

.

BROKEBACK MOUNTAIN EN TERRENO VEDADO PDF

ESFEROCITOSIS HEREDITARIA TRATAMIENTO PDF

.

Related Articles