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03/2010
A 12-year old girl was brought to the Dhaka Hospital of ICDDR,B with diarrhoea. Incidentally, the parents provided a history of repeated episodes of pallor and... 
Bangladesh | Anaemia | Haemolytic | Hereditary | Spherocytosis
Web Resource
Journal Article
Paediatrics and Child Health, ISSN 1751-7222, 08/2019, Volume 29, Issue 8, pp. 359 - 364
Hereditary spherocytosis is a red cell membrane disorder which is variable in respect to clinical presentation, biochemical and genetic basis. This review... 
jaundice | anaemia | cholelithiasis | haemolysis | hereditary spherocytosis | splenomegaly | Physiological aspects | Care and treatment | Spherocytosis, Hereditary | Diagnosis | Pediatric research
Journal Article
Medical Journal of Dr. D.Y. Patil University, ISSN 0975-2870, 01/2014, Volume 7, Issue 2, pp. 229 - 231
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a... 
Gallstones | spherocytosis | jaundice | splenomegaly
Journal Article
Paediatrics and Child Health, ISSN 1751-7222, 2015, Volume 25, Issue 8, pp. 381 - 386
Abstract Hereditary spherocytosis is a red cell membrane disorder which is heterogeneous in respect to clinical presentation, biochemical and genetic basis.... 
Pediatrics | jaundice | anaemia | cholelithiasis | haemolysis | hereditary spherocytosis | splenomegaly | Jaundice | Splenomegaly | Haemolysis | Anaemia | Cholelithiasis | Hereditary spherocytosis | Care and treatment | Spherocytosis | Risk factors
Journal Article
Acta Haematologica, ISSN 0001-5792, 2018, Volume 141, Issue 2, pp. 63 - 64
Journal Article
Transfusion clinique et biologique, ISSN 1246-7820, 2010, Volume 17, Issue 3, pp. 138 - 142
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in one or more of the proteins composing red blood cell... 
Thérapie | Therapy | Sphérocytose héréditaire | Hemolytic anemia | Anémie hémolytique | Hereditary spherocytosis | Membrane érythrocytaire | Red cell membrane | Diagnostic | Diagnosis | MANAGEMENT | BAND-3 | SPECTRIN | IMMUNOLOGY | HEMATOLOGY
Journal Article
FRONTIERS IN PHYSIOLOGY, ISSN 1664-042X, 07/2019, Volume 10, pp. 815 - 815
Hereditary spherocytosis (HS) is the most common red blood cell (RBC) membrane disorder causing hereditary hemolytic anemia. Patients with HS have defects in... 
ALLELE | PHYSIOLOGY | hereditary spherocytosis | ALPHA(LELY) | next generation sequencing | hydrops fetalis | alpha(LEPRA) | DEFICIENCY | SPTA1 | RED-CELL SPECTRIN | PROTEINS | alpha-spectrin | hemolytic anemia | Causes of | Complications and side effects | Care and treatment | Genetic aspects | Spherocytosis, Hereditary | Hemolytic anemia | Hydrops fetalis | Anemia | α-spectrin | αLEPRA
Journal Article
Journal of Glaucoma, ISSN 1057-0829, 12/2018, Volume 27, Issue 12, pp. e187 - e190
PURPOSE:To report a case of glaucoma and the inherited red cell membranopathy hereditary spherocytosis diagnosed simultaneously in 2 individuals in a family.... 
hereditary spherocytosis | glaucoma | glaucomatous optic neuropathy | OPHTHALMOLOGY | Glaucoma | Complications and side effects | Care and treatment | Spherocytosis, Hereditary | Risk factors
Journal Article
Journal of Pediatric Hematology/Oncology, ISSN 1077-4114, 2017, Volume 39, Issue 3, pp. 233 - 234
Moyamoya syndrome is an unusual cerebrovascular disorder, which has rarely been reported in association with hereditary spherocytosis. We present the case of a... 
hereditary spherocytosis | children | stroke | Moyamoya | ONCOLOGY | DISEASE | PEDIATRICS | HEMATOLOGY | Stroke - etiology | Humans | Male | Disease Management | Child | Moyamoya Disease - diagnosis | Moyamoya Disease - complications | Spherocytosis, Hereditary - complications | Index Medicus
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 06/2019, Volume 23, Issue 6, pp. 4454 - 4463
Journal Article