Cargando…

Difficulties in the diagnosis of HbS/beta thalassemia: Really a mild disease?

BACKGROUND: HbS/b cases having clinical, hematologic and electrophoretic similarities cannot be sufficiently distinguished from sickle cell anemia cases and are misdiagnosed as sickle cell anemia. This study will investigate the congruence between the HPLC thalassemia scanning tests and the laborato...

Descripción completa

Detalles Bibliográficos
Autores principales:	Uçucu, Süheyl, Karabıyık, Talha, Azik, Fatih
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Society of Medical Biochemists of Serbia, Belgrade 2022
Materias:	Original Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882016/ https://www.ncbi.nlm.nih.gov/pubmed/35291497 http://dx.doi.org/10.5937/jomb0-30420

Ejemplares similares

Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children
por: Belisário, André Rolim, et al.
Publicado: (2015)

HbS-Sicilian (δβ)(0)-Thalassemia: A Rare Variant of Sickle Cell
por: Onimoe, Grace, et al.
Publicado: (2017)

The compound state: Hb S/beta-thalassemia()
por: Figueiredo, Maria Stella
Publicado: (2015)

Simeprevir and Sofosbuvir Combination Treatment in a Patient with HCV Cirrhosis and HbS Beta 0-Thalassemia: Efficacy and Safety despite Baseline Hyperbilirubinemia
por: Papadopoulos, Nikolaos, et al.
Publicado: (2016)

Economic burden of beta-thalassemia/Hb E and beta-thalassemia major in Thai children
por: Riewpaiboon, Arthorn, et al.
Publicado: (2010)

Assessment of Myocardial Performance Index and Aortic Elasticity in Patients With Beta-Thalassemia Major
por: Sahin, Cem, et al.
Publicado: (2015)

Management of gingival hyperpigmentation induced by increased ferritin level in a HbS‐β(+) thalassemia patient using diode laser
por: Darkazali, Raneem, et al.
Publicado: (2023)

Abstract 40: Adrenal insufficiency in patients with HbE/Beta thalassemia
por: Singh, Arijit, et al.
Publicado: (2022)

The Properties of Red Blood Cells from Patients Heterozygous for HbS and HbC (HbSC Genotype)
por: Hannemann, A., et al.
Publicado: (2011)

Genotype–phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis
por: Traivaree, Chanchai, et al.
Publicado: (2018)

Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients
por: Cyrus, Cyril, et al.
Publicado: (2017)

Induction of fetal hemoglobin: Lentiviral shRNA knockdown of HBS1L in β(0)-thalassemia/HbE erythroid cells
por: Chumchuen, Sukanya, et al.
Publicado: (2023)

Cation Homeostasis in Red Cells From Patients With Sickle Cell Disease Heterologous for HbS and HbC (HbSC Genotype)
por: Hannemann, A., et al.
Publicado: (2015)

A decision support scheme for beta thalassemia and HbE carrier screening
por: Das, Reena, et al.
Publicado: (2020)

Thalidomide-Induced Primary Amenorrhea in a Patient With HbE/Beta-Thalassemia
por: Singha, Arijit, et al.
Publicado: (2023)

Hematological and molecular analyses of the HbS allele among the Sudanese population
por: Khalafallah, Tariq Osman, et al.
Publicado: (2022)

The effect of measurement area size on the reliability of myocardial iron load measurement in cardiac magnetic resonance imaging examinations of thalassemia patients
por: YENİÇERİ, İbrahim Önder, et al.
Publicado: (2021)

HbS Binding to GP1bα Activates Platelets in Sickle Cell Disease
por: Annarapu, Gowtham K., et al.
Publicado: (2016)

Fetal heterozygosity for both Hb G-Hsi-Tsou and beta thalassemia: A case report
por: Alhazidou, Elena, et al.
Publicado: (2020)

Hydroxyurea decreases hospitalizations in pediatric patients with Hb SC and Hb SB+ thalassemia
por: Lebensburger, Jeffrey D, et al.
Publicado: (2015)

Mitochondrial Changes in β(0)-Thalassemia/Hb E Disease
por: Khungwanmaythawee, Kornpat, et al.
Publicado: (2016)

Measurement of HbA(1c) and HbA(2) by Capillarys 2 Flex Piercing HbA(1c) programme for simultaneous management of diabetes and screening for thalassemia
por: Ke, Peifeng, et al.
Publicado: (2017)

Predictive SNPs for β(0)-thalassemia/HbE disease severity
por: Munkongdee, Thongperm, et al.
Publicado: (2021)

Beta-thalassemia
por: Galanello, Renzo, et al.
Publicado: (2010)

Challenges in the Diagnosis of Beta-thalassemia Syndrome: The Importance of Molecular Diagnosis
por: Rameli, Nabilah, et al.
Publicado: (2022)

Gastric cancer with situs inversus totalis: does it really create difficulties for surgeons?
por: Gündeş, Ebubekir, et al.
Publicado: (2018)

The Effect of Alpha Thalassemia, HbF and HbC on Haematological Parameters of Sickle Cell Disease Patients in Ibadan, Nigeria
por: Fasola, Foluke Atinuke, et al.
Publicado: (2022)

HB E/β°Thalassemia can present with normal phenotype
por: Pal, Ranabir, et al.
Publicado: (2010)

Glutathione Redox System in β-Thalassemia/Hb E Patients
por: Kalpravidh, Ruchaneekorn W., et al.
Publicado: (2013)

Low HbA2 Level in β-Thalassemia Trait
por: ÖZSOYLU, Şinasi
Publicado: (2013)

Moyamoya syndrome in a child with HbEβ‐thalassemia
por: Zahra, Akmal, et al.
Publicado: (2022)

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
por: Giardine, Belinda, et al.
Publicado: (2014)

Is COVID in Neonates Really Mild?
por: Khamkar, Anilkumar M., et al.
Publicado: (2021)

Socio-religious Prognosticators of Psychosocial Burden of Beta Thalassemia Major
por: ul Hassan Rashid, Muhammad Abo, et al.
Publicado: (2020)

CNTO 530 Increases Expression of HbA and HbF in Murine Models of β-Thalassemia and Sickle Cell Anemia
por: Makropoulos, Dorie A, et al.
Publicado: (2013)

Prolonged Pyrexia: Kikuchi-Fujimoto Disease in a Patient With Hb H-Constant Spring Thalassemia
por: Kasinathan, Ganesh
Publicado: (2020)

Shared molecular basis, diagnosis, and co-inheritance of alpha and beta thalassemia
por: Khatri, Govinda, et al.
Publicado: (2021)

5613312 PLASMATIC MICROPARTICLES AS POTENTIAL BIOMARKERS IN THE PREVENTIVE DIAGNOSIS OF BETA THALASSEMIA
por: Chebbi, M., et al.
Publicado: (2023)

Life satisfaction and difficulties experienced by the family members of individuals with thalassemia
por: Sevinç, Sibel
Publicado: (2023)

Significance of borderline HbA(2) levels in β thalassemia carrier screening
por: Colaco, Stacy, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_mhp0ef7e5gjutf5j1in287bko7