Literature DB >> 22055020

Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.

Paula H B Bolton-Maggs1, Jacob C Langer, Achille Iolascon, Paul Tittensor, May-Jean King.   

Abstract

Guidelines on hereditary spherocytosis (HS) published in 2004 (Bolton-Maggs et al, 2004) are here replaced to reflect changes in current opinion on the surgical management, (particularly the indications for concomitant splenectomy with cholecystectomy in children with mild HS, and concomitant cholecystectomy with splenectomy in those with asymptomatic gallstones). Further potential long term hazards of splenectomy are now recognised. Advances have been made in our understanding of the biochemistry of the red cell membrane which underpins the choice of tests. Biochemical assays of membranes proteins and genetic analysis may be indicated (rarely) to diagnose atypical cases. The diagnostic value of the eosin-5-maleimide (EMA) binding test has been validated in a number of studies with understanding of its limitations.
© 2011 Blackwell Publishing Ltd.

Entities:  

Mesh:

Year:  2011        PMID: 22055020     DOI: 10.1111/j.1365-2141.2011.08921.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  69 in total

1.  Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study.

Authors:  Thomas Pincez; Corinne Guitton; Frédéric Gauthier; Guénolée de Lambert; Véronique Picard; Madeleine Fénéant-Thibault; Ali Turhan; Narla Mohandas; Gil Tchernia; Loïc Garçon
Journal:  Blood       Date:  2016-01-15       Impact factor: 22.113

Review 2.  Abnormalities of the erythrocyte membrane.

Authors:  Patrick G Gallagher
Journal:  Pediatr Clin North Am       Date:  2013-10-15       Impact factor: 3.278

3.  Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up.

Authors:  B A I Attalla; Z A Karrar; G Ibnouf; A O Mohamed; O Abdelwahab; E M Nasir; M A El Seed
Journal:  Afr Health Sci       Date:  2013-03       Impact factor: 0.927

4.  Laparoscopic splenectomy in patients with hereditary spherocytosis: report on 12 consecutive cases.

Authors:  R Vecchio; Eva Intagliata; F Ferla; S Marchese; R R Cacciola; E Cacciola
Journal:  Updates Surg       Date:  2013-10-16

5.  A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.

Authors:  Chao Wang; Yazhou Cui; Yan Li; Xiao Liu; Jinxiang Han
Journal:  Intractable Rare Dis Res       Date:  2015-05

Review 6.  A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Authors:  Robert D Christensen; Hassan M Yaish; Patrick G Gallagher
Journal:  Pediatrics       Date:  2015-06       Impact factor: 7.124

7.  Testing for hereditary spherocytosis: a French experience.

Authors:  Caroline Mayeur-Rousse; Mélanie Gentil; Jérémie Botton; Madeleine Fénéant Thibaut; Corinne Guitton; Véronique Picard
Journal:  Haematologica       Date:  2012-12       Impact factor: 9.941

8.  Coexistence of gilbert syndrome and hereditary spherocytosis in a child presenting with extreme jaundice.

Authors:  Jae Hee Lee; Kyung Rye Moon
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2014-12-31

9.  Hereditary spherocytosis diagnosed with extremely low glycated hemoglobin compared to plasma glucose levels.

Authors:  Takuya Okamoto; Hisato Shima; Yoshihiko Noma; Machiko Komatsu; Hiroyuki Azuma; Keiko Miya; Manabu Tashiro; Tomoko Inoue; Chiaki Masaki; Hiroaki Tada; Norimichi Takamatsu; Jun Minakuchi
Journal:  Diabetol Int       Date:  2020-07-12

Review 10.  New insights on hereditary erythrocyte membrane defects.

Authors:  Immacolata Andolfo; Roberta Russo; Antonella Gambale; Achille Iolascon
Journal:  Haematologica       Date:  2016-10-18       Impact factor: 9.941

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.