Literature DB >> 31823208

Laboratory Approach to Hemolytic Anemia.

Manu Jamwal1, Prashant Sharma1, Reena Das2.   

Abstract

Hemolytic anemias are a group of disorders with varied clinical and molecular heterogeneity. They are characterized by decreased levels of circulating erythrocytes in blood. The pathognomic finding is a reduced red cell life span with severe anemia or, compensated hemolysis accompanied by reticulocytosis. The diagnostic workup or laboratory approach for hemolytic anemias is based on methodical step-wise testing which includes red blood cell morphology, hematological indices with increased reticulocyte count along with clinical features of hemolytic anemias. If conventional laboratory tests are unable to detect the underlying cause of hemolysis, genetic testing is recommended. Sanger sequencing along with conventional testing is the most efficient way to diagnose the underlying genetic causes, especially in thalassemias/hemoglobinopathies, if required. However, hemolytic anemias being highly heterogeneous disorders, next-generation sequencing-based screening is rapidly becoming an efficient way to decipher the etiologies where common causes have been excluded.

Entities:  

Keywords:  Hemoglobinopathy; Hemolytic anemia; Laboratory investigations; Red cell disorders; Red cell enzyme deficiencies

Mesh:

Substances:

Year:  2019        PMID: 31823208     DOI: 10.1007/s12098-019-03119-8

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  43 in total

1.  Thrombo-embolic disease after splenectomy for hereditary stomatocytosis.

Authors:  G W Stewart; J A Amess; S W Eber; C Kingswood; P A Lane; B D Smith; W C Mentzer
Journal:  Br J Haematol       Date:  1996-05       Impact factor: 6.998

2.  PK-LR gene mutations in pyruvate kinase deficient Portuguese patients.

Authors:  L Manco; M L Ribeiro; H Almeida; O Freitas; A Abade; G Tamagnini
Journal:  Br J Haematol       Date:  1999-06       Impact factor: 6.998

3.  Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR gene.

Authors:  Elisa Fermo; Paola Bianchi; Laurent R Chiarelli; Frederic Cotton; Cristina Vercellati; Karin Writzl; Kerry Baker; Ian Hann; Robin Rodwell; Giovanna Valentini; Alberto Zanella
Journal:  Br J Haematol       Date:  2005-06       Impact factor: 6.998

4.  Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant.

Authors:  Manu Jamwal; Anu Aggarwal; Anirban Das; Arindam Maitra; Prashant Sharma; Shekhar Krishnan; Neeraj Arora; Deepak Bansal; Reena Das
Journal:  Clin Chim Acta       Date:  2017-02-20       Impact factor: 3.786

5.  Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia.

Authors:  M J King; J Behrens; C Rogers; C Flynn; D Greenwood; K Chambers
Journal:  Br J Haematol       Date:  2000-12       Impact factor: 6.998

6.  Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

Authors:  May-Jean King; Paul Telfer; Heather MacKinnon; Lisa Langabeer; Corrina McMahon; Philip Darbyshire; Didier Dhermy
Journal:  Cytometry B Clin Cytom       Date:  2008-07       Impact factor: 3.058

Review 7.  Hereditary red cell membrane disorders and laboratory diagnostic testing.

Authors:  M-J King; A Zanella
Journal:  Int J Lab Hematol       Date:  2013-03-11       Impact factor: 2.877

Review 8.  Next-generation sequencing in the clinic: are we ready?

Authors:  Leslie G Biesecker; Wylie Burke; Isaac Kohane; Sharon E Plon; Ron Zimmern
Journal:  Nat Rev Genet       Date:  2012-11       Impact factor: 53.242

9.  Peas, beans, and the Pythagorean theorem - the relevance of glucose-6-phosphate dehydrogenase deficiency in dermatology.

Authors:  Oliver Brandt; Armin Rieger; Alexandra Geusau; Georg Stingl
Journal:  J Dtsch Dermatol Ges       Date:  2008-04-07       Impact factor: 5.584

Review 10.  Red blood cell PK deficiency: An update of PK-LR gene mutation database.

Authors:  Giulia Canu; Maria De Bonis; Angelo Minucci; Ettore Capoluongo
Journal:  Blood Cells Mol Dis       Date:  2016-01-12       Impact factor: 3.039

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  4 in total

1.  Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis.

Authors:  Manu Jamwal; Nabhajit Mallik; Arun Vijayalakshmi Aravindan; Arihant Jain; Prashant Sharma; Pankaj Malhotra; Reena Das
Journal:  Ann Hematol       Date:  2020-10-08       Impact factor: 3.673

2.  Clinical-Pathological Conference Series from the Medical University of Graz : Case No 174: A 25-year-old pregnant woman from Afghanistan with headache and a blast flag in the automated differential blood count.

Authors:  Philipp K Bauer; Peter Krippl; Elisabeth Fabian; Karoline I Mayer-Pickel; Robert Krause; Franz Bauer; Guenter J Krejs
Journal:  Wien Klin Wochenschr       Date:  2020-07       Impact factor: 1.704

Review 3.  The diagnostic protocol for hereditary spherocytosis-2021 update.

Authors:  Yangyang Wu; Lin Liao; Faquan Lin
Journal:  J Clin Lab Anal       Date:  2021-10-24       Impact factor: 2.352

4.  Individual-and community-level factors associated with anemia among children aged 6-23 months in sub-Saharan Africa: evidence from 32 sub-Saharan African countries.

Authors:  Beminate Lemma Seifu; Getayeneh Antehunegn Tesema
Journal:  Arch Public Health       Date:  2022-08-06
  4 in total

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