Results 71 to 80 of about 11,856 (183)

Haemoglobinopathies and health disparities: findings of a large-scale sample survey among indigenous populations in Odisha, India

BMJ Open
Objectives To estimate the prevalence of sickle cell trait, sickle cell disease, beta-thalassaemia minor and beta-thalassaemia major among Odisha’s indigenous populations and to examine associated haematological profiles and survival outcomes based on ...
Sanghamitra Pati, Jaya Singh Kshatri, Debdutta Bhattacharya, Sneha Singh, Haimanti Bhattacharya, Rachita Pradhan, A K Kavitha   +6 more
doaj   +1 more source

Sickle Cell Trait Causing Splanchnic Venous Thrombosis

Case Reports in Hepatology, 2015
Sickle cell trait is considered as a benign condition as these individuals carry only one defective gene and typically have their life span similar to the normal population without any health problems related to sickle cell. Only under extreme conditions,
Priyanka Saxena, Pratibha Dhiman, Chhagan Bihari, Archana Rastogi   +3 more
doaj   +1 more source

Sickle-cell Trait in Africans [PDF]

BMJ, 1952
Henry Foy, Athena Kondi
openaire   +2 more sources

The sickle cell trait and end stage renal disease in Salvador, Brazil.

PLoS ONE, 2018
BACKGROUND:Carriers of the sickle cell trait (HbAS) usually remain asymptomatic. However, under conditions of low tissue oxygenation, red blood cell sickling and vascular obstruction may develop.
Dona J Alladagbin, Paula N Fernandes, Maria B Tavares, Jean T Brito, Geraldo G S Oliveira, Luciano K Silva, Nadia A Khouri, Marilia B Oliveira, Tatiana Amorim, Cácia M Matos, Guilherme S Ribeiro, Antônio A Lopes, Marilda S Gonçalves, Washington L C Dos-Santos   +13 more
doaj   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Sickled erythrocytes in urine as a clue to the diagnosis of sickle cell trait

Saudi Journal of Kidney Diseases and Transplantation, 2017
Sickled erythrocytes in patients of sickle cell trait with microscopic hematuria have rarely been reported so far. A 30-year-old female underwent delivery of a healthy full-term baby by cesarean section. However, postcesarean, she had pain in abdomen and
Shanu Srivastava, Rashmi Srivastava, K G Ghorpade   +2 more
doaj  

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Serum Lactate Dehydrogenase in Children with Sickle cell disease.

Nigerian Journal of Paediatrics
Summary: Measurement of scrum LDH is frequently employed diagnostically in disease states associated with tissue destructions of various types. Since children with sickle cell disease suffer from chronic red cell destruction and associated necrosis of ...
Adebonojo Festus O.
doaj  

Prevalence Of Common Hemoglobinopathies in Gujarat: An Analysis of a Large Population Screening Program

National Journal of Community Medicine, 2012
Objectives: To determine prevalence and geographical distribution of ß-thalassemia trait and sickle cell trait in Gujarat Methods: The present study includes 3, 17,539 persons who were screened for hemoglobinopathies from September 2004 to November ...
Ashwin P Patel , Madhuben R Naik , Nilam M Shah , Narmadeshwar P Sharma , Prakash H Parmar   +4 more
doaj  

International flight-associated splenic infarction in a 33-year-old man with sickle cell trait. [PDF]

CMAJ
Chadelat A, Tassart M, Bachmeyer C.
europepmc   +1 more source