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
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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 Hemolysis. 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. .. Sumner G. Hunnewell. Number of variety of hereditary societies. Based on.... descent of a single person (Charlemagne, Elder William Brewster). the qualities of a single person (Cincinnati, Colonial Cavaliers). Polyposis. Syndromes in the Mediterranean Region. Thomas M Attard MD FAAP FACG. Associate Professor, Pediatrics, Gastroenterology, University of Malta, Malta. . Consultant Gastroenterologist Children’s Mercy Hospital, Kansas MO, USA.. UterineCancerMost people develop uterine cancer by chance or as a result of risk factors that occur over the course of a lifetime However up to 10percentof people who are diagnosed with uterine cancer 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. –. Uterine Cancer Most people develop uterine cancer by chance or as a result of risk factors that occur over the course of a lifetime. However, up to 10 % ( percent ) of people who are diagnosed with 1, 2]. Table shows the genetic basis of most common membrane defects. Glucose-6-phosphate dehydrogenase (G6PD) and pyruvate kinase (PK), are the most common enzyme deciencies, showing an X-linked an 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 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 Lab 4. What is osmosis? . a process by which molecules of a solvent tend to pass through a semi-permeable membrane from a less concentrated solution into a more concentrated one.. Osmotic fragility of RBCs .
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