PPT-Diagnosis and Management of Hereditary Spherocytosis in Neonates

Author : grace3 | Published Date : 2023-11-19

Israel Neonatology Association Robert Christensen MD A heterogeneous disorder where abnormalities of RBC structural proteins lead to loss of RBC membrane

Presentation Embed Code

Download Presentation

Download Presentation The PPT/PDF document "Diagnosis and Management of Hereditary S..." is the property of its rightful owner. Permission is granted to download and print the materials on this website for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.

Diagnosis and Management of Hereditary Spherocytosis in Neonates: Transcript


Israel Neonatology Association Robert Christensen MD A heterogeneous disorder where abnormalities of RBC structural proteins lead to loss of RBC membrane surface area Sphericalshaped. 1 Hereditary Spherocytosis The British Committee for Standards in Haematology Address for correspondence: Dr. Paula Bolton - Maggs c/ o BCSH Administrator British Society for Haematology 100 White L What is the APGAR Score? . When is it taken?. Child Development. Book Reviews. Reality Baby. Ahlai. Zack. Lu. Jordan. Shante. Susana P.. Lu G.. NEXT TIME- Friday. . Sierra M.. . Kaitlyn. C.. Reality Baby ~ Tuesday-Thursday. TULIP. Theory. T. otal Hereditary Depravity. . . Man’s nature is corrupt. . No ability to choose good over evil. U. nconditional Election. . . God’s choice – A few saved. . All others excluded from salvation. Robert A. Somer, MD. Head, Medical Oncology and Hematology. Director, Office of Clinical Research. MD Anderson Cancer Center- Cooper. What is Cancer?. Official Definition: A malignant proliferation of cells that is a result of a . Page 1of 26UnitedHealthcare Commercial Medical PolicyEffective 01/01/2021Proprietary Information of UnitedHealthcare Copyright 2021United HealthCare Services IncUnitedHealthcareCommercial MedicalPolic Neonatal Neutropenia: . By : Dr. Mahdi Shahriari. Pediatric Hematologist Oncologist. Associate Professor of Shiraz University of Medical Sciences. 1396. Objectives. Summarize the differential diagnosis of leukopenia in a neonate.. Alaa duhair , Alaa alhoubi ,Shimaa Alshakhe.. Under the supervision of . : MS. . Ibtisam. Alaswad .. A 27-year-old woman presented with recurrent abdominal swelling, . She has had four units of blood transfusion in childhood; her last transfusion was 10 years prior to presentation. She also has recurrent yellowish discoloration of the eyes., mildly pale, moderately jaundiced and has a gnathopathy. The spleen was enlarged by 6cm but the liver was not palp large. Laboratory investigation shows a hematocrit of 0.27 (Hb 9g/. is defined as the premature destruction of red blood cells (RBCs).. Anemia results when the rate of destruction exceeds the capacity of the marrow to produce RBCs. Normal RBC survival time is 110. –. Jeff Kaufhold MD FACP. March 2015. Hereditary Disease of the kidneys - Summary. Glomerular diseases. Hereditary Cystic Diseases. Hereditary . Nephroses. Wilms. Tumor. Reflux Nephropathy. Hereditary Stone Diseases. Dr Bijan Keikhaei. Full Professor of Pediatric . Hematology and Oncology. Research Center for Thalassemia and Hemoglobinopathy, Health Institute, Ahvaz Jundishapur University of Medical Sciences. Introduction. th Annual Scientific Meeting of Page | 26 Gulf Medical University, 5 th & 6 th November, 2014 Hasmukh Gala * , Edwin D’souza, Mahmoud Shamsheldeen Department of Pediatrics, Gulf Medical College Ho Posted on Friday, March 12, 2004 DURHAM, N.C. -- Two seemingly disparate hereditary syndromes actually stem, in some patients, from a uke University Medical Center genejuvenile polyposis -- characteri Angioedema of the Larynx: Averting Death Nikhil Rajan 1 , Vidhu Sharma 1 , Sourabha Kumar Patro 2 , Amit Goyal 1 1 Department of Otorhinolaryngology, All India Institute of Medical Sciences, Jodhpur, To the Editor,Coinheritance of hereditary spherocytosis ,HS) thalassemia is very rare. HS is a familial haemolytic disorder resulting from primary abnormality of red cell membrane. It is transmitted

Download Document

Here is the link to download the presentation.
"Diagnosis and Management of Hereditary Spherocytosis in Neonates"The content belongs to its owner. You may download and print it for personal use, without modification, and keep all copyright notices. By downloading, you agree to these terms.

Related Documents