Cargando…

The XmnI polymorphic site 5’ to the gene G(γ) in a Brazilian patient with sickle cell anaemia – fetal haemoglobin concentration, haematology and clinical features

We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic manifestations of sickle cell anaemia, only pain crises of a mild intensity. After lab...

Descripción completa

Detalles Bibliográficos
Autores principales:	Belini Júnior, Édis, Cançado, Rodolfo D., Domingos, Claudia R.B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Termedia Publishing House 2010
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298355/ https://www.ncbi.nlm.nih.gov/pubmed/22419945 http://dx.doi.org/10.5114/aoms.2010.17101

Ejemplares similares

XmnI polymorphism frequency in heterozygote beta thalassemia subjects and its relation to Fetal hemoglobin levels
por: Chinelato, Isabela Sandrin, et al.
Publicado: (2011)

Association between XmnI Polymorphism and HbF Level in Sickle Cell Disease Patients from Chhattisgarh
por: Bhagat, Sanjana, et al.
Publicado: (2012)

Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients
por: Motovali-Bashi, Majid, et al.
Publicado: (2015)

EF Bart's Disease with Coinheritance of Gγ-XmnI and Aγ-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia
por: Laks, Kane M., et al.
Publicado: (2020)

Comet Assay as a technique to evaluate DNA damage in sickle cell anemia patients
por: Barberino, Willian Marcel, et al.
Publicado: (2012)

A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia
por: Adeyemo, Titilope A., et al.
Publicado: (2018)

The influence of hydroxyurea on oxidative stress in sickle cell anemia
por: Torres, Lidiane de Souza, et al.
Publicado: (2012)

Modulating Effect of the −158 (G)γ (C→T) Xmn1 Polymorphism in Indian Sickle Cell Patients
por: Pandey, Sanjay, et al.
Publicado: (2012)

Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia
por: Kumkhaek, Chutima, et al.
Publicado: (2008)

Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia
por: Tshilolo, L., et al.
Publicado: (2012)

Foetal Haemoglobin and Disease Severity in Nigerian Children with Sickle Cell Anaemia
por: Adeodu, Oluwagbemiga O., et al.
Publicado: (2017)

Haematological Profile of Children With Sickle Cell Anaemia in Steady State
por: Aliu, Rasaki, et al.
Publicado: (2020)

Foetal haemoglobin and disease severity in sickle cell anaemia patients in Kampala, Uganda
por: Mpalampa, Lena, et al.
Publicado: (2012)

Fetal‐haemoglobin enhancing genotype at BCL11A reduces HbA(2) levels in patients with sickle cell anaemia
por: Adeyemo, Titilope A., et al.
Publicado: (2021)

Haemoglobin and anaemia in the SMART study
por: Mocroft, A, et al.
Publicado: (2010)

FOETAL HAEMOGLOBIN (HbF) STATUS IN ADULT SICKLE CELL ANAEMIA PATIENTS IN IBADAN, NIGERIA
por: Olaniyi, J.A., et al.
Publicado: (2010)

Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran
por: Miri-Moghaddam, Ebrahim, et al.
Publicado: (2017)

Thalassemia Major and Intermedia Patients in East Java do not Show Fetal Hemoglobin Level Difference in Relation to XMNI Polymorphism
por: Wulandari, Retno Dwi, et al.
Publicado: (2020)

Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Study
por: Renoux, Céline, et al.
Publicado: (2016)

Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia
por: Silva, Danilo Grunig Humberto, et al.
Publicado: (2013)

Sickle haemoglobin, haemoglobin C and malaria mortality feedbacks
por: Gonçalves, Bronner P., et al.
Publicado: (2016)

Haematological values in homozygous sickle cell disease in steady state and haemoglobin phenotypes AA controls in Lagos, Nigeria
por: Akinbami, Akinsegun, et al.
Publicado: (2012)

Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia
por: Pereira-Martins, Diego A., et al.
Publicado: (2021)

HAEMATOLOGICAL PROFILE AND BLOOD TRANSFUSION PATTERN OF PATIENTS WITH SICKLE CELL ANAEMIA VARY WITH SPLEEN SIZE
por: Fasola, F.A., et al.
Publicado: (2019)

The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients
por: Pirozzi, Flavio Fontes, et al.
Publicado: (2018)

Nocturnal haemoglobin oxygen saturation variability is associated with vitamin C deficiency in Tanzanian children with sickle cell anaemia
por: Cox, SE, et al.
Publicado: (2011)

Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein
por: Torres, Lidiane S., et al.
Publicado: (2016)

Correction: Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein
por: Torres, Lidiane S., et al.
Publicado: (2017)

Bacteraemia in sickle cell anaemia is associated with low haemoglobin: a report of 890 admissions to a tertiary hospital in Tanzania
por: Makani, Julie, et al.
Publicado: (2015)

Assessing the Impact of COVID-19 Vaccines on Sickle Cell Anaemia Patients: A Comparative Analysis of Biochemical and Haematological Parameters
por: Aldali, Jehad A., et al.
Publicado: (2023)

Sickle Cell Anaemia Prevalence among Newborns in the Brazilian Amazon-Savanna Transition Region
por: Souza, Rayane Cristina, et al.
Publicado: (2019)

Sickle cell disease: looking back but towards the future
por: Cançado, Rodolfo Delfini
Publicado: (2012)

Intravenous ferric carboxymaltose for the treatment of iron deficiency anaemia – reply
por: Cancado, Rodolfo Delfini, et al.
Publicado: (2020)

Sickle Cell Anaemia and Malaria
por: Luzzatto, Lucio
Publicado: (2012)

Sickle Cell Anæmia in India
Publicado: (1952)

The Anæmias in Pregnancy: A Hæmatological, Clinical and Statistical Study
por: Choudhury, Sujata, et al.
Publicado: (1938)

Nocturnal haemoglobin oxygen desaturation in urban and rural East African paediatric cohorts with and without sickle cell anaemia: a cross-sectional study
por: L'Esperance, VS, et al.
Publicado: (2016)

Comprehensive healthcare for individuals with sickle cell disease - a constant challenge
por: Cançado, Rodolfo Delfini
Publicado: (2011)

Haemoglobin, anaemia, dementia and cognitive decline in the elderly, a systematic review
por: Peters, Ruth, et al.
Publicado: (2008)

Anaemia, Haemoglobin Level and Cause-Specific Mortality in People with and without Diabetes
por: Kengne, Andre Pascal, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_bqo976cat5gjrj6mv0k5tl76f7