Literature DB >> 27423233

Sickle Cell Trait: A Benign State?

Taiwo R Kotila1.   

Abstract

BACKGROUND: Sickle cell trait (SCT) is the heterozygous form of sickle cell disease and expectedly should be a benign state with no complications ascribed to it. There are numerous reports challenging its being a benign condition, though this is controversial. METHODS AND
RESULTS: A review of the results of the accompanying investigations done on some of the patients show that beta thalassemia may be responsible for many of the ascribed symptoms and complications. These patients may therefore have sickle cell beta thalassemia, a compound heterozygous form of sickle cell disease.
CONCLUSION: It is important to screen for beta thalassemia using red cell indices and quantitation of the different hemoglobin fractions before attributing any symptoms to SCT. DNA analysis, though useful in ascertaining the presence of the sickle cell gene, is not sufficient. There is the need to exclude the presence of mutations for beta thalassemia, which often is geographical region-specific.
© 2016 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2016        PMID: 27423233     DOI: 10.1159/000446526

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  4 in total

1.  Chronic Disease Management in Sickle Cell Trait Patients in the Primary Care Setting: A Case Report.

Authors:  Rachel N Fields; Suzanne Minor
Journal:  Cureus       Date:  2020-10-30

2.  The impact of HBB-related hemoglobinopathies carrier status on fetal fraction in noninvasive prenatal screening.

Authors:  Manesha Putra; Kristjan Eerik Kaseniit; Melissa A Hicks; Dale Muzzey; David Hackney
Journal:  Prenat Diagn       Date:  2022-03-23       Impact factor: 3.242

Review 3.  Sickle cell trait and the potential risk of severe coronavirus disease 2019-A mini-review.

Authors:  Tawakalitu Abosede Kehinde; Mayowa Azeez Osundiji
Journal:  Eur J Haematol       Date:  2020-07-14       Impact factor: 3.674

4.  Spontaneous splenic rupture, mesenteric ischemia and spinal infarction after aortic repair for acute type A dissection in a patient with sickle cell trait.

Authors:  Makoto Toyoda; Tadashi Kitamura; Kouki Nakashima; Yoshikiyo Matsunaga; Masaki Nie; Kagami Miyaji
Journal:  Gen Thorac Cardiovasc Surg       Date:  2020-10-22
  4 in total

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