• Treatment of the inherited blood disorder thalassemia depends upon the level of severity. For mild forms of the condition, advice and counseling are often...
    41 KB (4,621 words) - 22:13, 27 May 2025
  • Thumbnail for Thalassemia
    Thalassemias are a group of inherited blood disorders that manifest as the production of reduced hemoglobin. Symptoms depend on the type of thalassemia...
    75 KB (7,679 words) - 03:28, 23 April 2025
  • Thumbnail for Beta thalassemia
    Beta-thalassemia (β-thalassemia) is an inherited blood disorder, a form of thalassemia resulting in variable outcomes ranging from clinically asymptomatic...
    36 KB (6,284 words) - 10:18, 28 May 2025
  • Alpha-thalassemia (α-thalassemia, α-thalassaemia) is an inherited blood disorder and a form of thalassemia. Thalassemias are a group of inherited blood...
    33 KB (4,411 words) - 08:38, 21 March 2025
  • Thumbnail for Microcytic anemia
    made by DNA analysis for alpha thalassemia and hemoglobin electrophoresis for beta thalassemia. Management of thalassemia involves life-long blood transfusions...
    16 KB (1,710 words) - 12:47, 24 May 2025
  • Thumbnail for Transfusion-dependent anemia
    anemia, most notably myelodysplastic syndromes (MDS) and thalassemia. Due to the number of diseases that can cause transfusion-dependent anemia, diagnosing...
    25 KB (2,854 words) - 12:54, 23 May 2025
  • list of Non-governmental organization (NGOs) based in Karachi, Sindh, Pakistan. List of NGOs in Pakistan List of NGOs Based in Karachi List of NGOs in...
    4 KB (31 words) - 08:07, 29 January 2025
  • CRISPR Therapeutics (category Biotechnology companies of Switzerland)
    commercialize medicines for various diseases including sickle cell disease, beta thalassemia, various cancers, type 1 diabetes, and cardiovascular diseases. The CEO...
    11 KB (920 words) - 11:02, 28 May 2025
  • Hemoglobin D (category CS1 maint: DOI inactive as of November 2024)
    heterozygous (inherited in only one of the chromosome 11) HbD trait, HbD-thalassemia, HbS-D (sickle cell) disease, and, very rarely, homozygous (inherited...
    33 KB (3,699 words) - 22:49, 22 May 2025
  • Thumbnail for Hemoglobin A
    to have a “silent” α-thalassemia whereas, if the mutation is on both then it is considered an α-thalassemia trait. α-thalassemia is mostly found in sub-tropical...
    17 KB (2,067 words) - 20:33, 28 December 2024
  • organisation. It is a youth organisation working for blood donation, thalassemia, bone marrow transplantation and disaster relief.[citation needed] Since...
    11 KB (874 words) - 17:55, 29 April 2025
  • Thumbnail for Fetal hemoglobin
    Fetal hemoglobin (category Embryology of cardiovascular system)
    hemoglobin begin to be produced. Diseases such as beta thalassemias, which affect components of the adult hemoglobin, can delay this process, and cause...
    38 KB (4,538 words) - 10:54, 4 March 2025
  • Shantilal C. Sheth (category Fellows of the Royal College of Physicians)
    presentation during PEDICON 2006, Delhi, January 6th, 2006. Progress in the management of thalassemia". Indian Pediatrics. 43 (6): 503–6. PMID 16820659....
    9 KB (788 words) - 08:37, 28 May 2025
  • Thumbnail for Jaundice
    guide to diagnosis and management. McGraw-Hill Professional. pp. 146–. ISBN 978-0-07-144035-6. Retrieved 15 November 2010. "Thalassemia". The Lecturio Medical...
    48 KB (5,076 words) - 13:07, 19 May 2025
  • Thumbnail for Sickle cell trait
    Sickle cell trait (category Disorders of globin and globulin proteins)
    presence of alpha-thalassemia has been shown to act protectively against microvasculatory distress before, during, and after exercise. Because of the microcirculatory...
    26 KB (2,894 words) - 19:29, 25 May 2025
  • Thumbnail for Anemia
    deficiency, folate deficiency, vitamin B12 deficiency, thalassemia and a number of bone marrow tumors. Causes of increased breakdown include genetic disorders...
    88 KB (9,069 words) - 12:24, 27 March 2025
  • Thumbnail for Splenectomy
    as sickle cell anemia or thalassemia. The spleen is an organ located in the abdomen next to the stomach. It is composed of red pulp which filters the...
    16 KB (1,838 words) - 21:50, 13 May 2025
  • Thumbnail for Hemoglobin electrophoresis
    used to investigate thalassemias, which are disorders caused by defective hemoglobin production. The test uses the principles of gel electrophoresis to...
    5 KB (540 words) - 13:30, 12 July 2024
  • State-Based Recommendations for Management of Alpha Thalassemia Trait and Silent Carrier Detected on the Newborn Screen". The Journal of Pediatrics. 195: 283–287...
    9 KB (1,049 words) - 04:38, 28 April 2024
  • the type of thalassemia and can vary from none to severe. Often there is mild to severe anemia (low red blood cells or hemoglobin) as thalassemia can affect...
    20 KB (1,900 words) - 14:29, 24 May 2025
  • Thumbnail for Sickle cell disease
    incidence of SCD and thalassemia. In Bahrain, a study published in 1998 that covered about 56,000 people in hospitals in Bahrain found that 2% of newborns...
    131 KB (14,213 words) - 10:05, 28 May 2025
  • Thumbnail for Craniotabes
    vitamin D deficiency), marasmus, syphilis, or thalassemia, can cause craniotabes if present during a time of rapid skull growth (most especially during gestation...
    6 KB (534 words) - 04:32, 25 May 2025
  • Thumbnail for Hydrops fetalis
    (2009-01-01). "Alpha thalassemia major--new mutations, intrauterine management, and outcomes". Hematology. American Society of Hematology. Education...
    15 KB (1,646 words) - 12:36, 28 March 2025
  • Thumbnail for Rachitic rosary
    cause of rachitic rosary, however its presence has also been noted in tumor-induced osteomalacia, primary hyperparathyroidism, and beta-thalassemia. It...
    8 KB (734 words) - 01:48, 27 May 2025
  • against him on publicly humiliating a disabled employee. The addition of thalassemia as a new disability under this new law allowed a Chhattisgarh girl with...
    20 KB (1,790 words) - 21:07, 18 October 2024
  • Thumbnail for Hemoglobin Lepore syndrome
    Hemoglobin Lepore syndrome (category Disorders of globin and globulin proteins)
    findings bear close resemblance to those of the beta-thalassemia trait; a blood disorder that reduces the production of the iron-containing protein hemoglobin...
    11 KB (1,230 words) - 02:11, 7 July 2024
  • Thumbnail for Priapism
    Causes of low-flow priapism include sickle cell anemia (most common in children), leukemia, and other blood dyscrasias such as thalassemia and multiple...
    21 KB (2,110 words) - 02:47, 29 October 2024
  • Thumbnail for Monash Medical Centre
    Monash Medical Centre (category Buildings and structures in the City of Monash)
    surgery. It is the statewide provider of Thalassemia services, for both children and adult populations. Most of the services are provided on an outpatient...
    11 KB (1,113 words) - 11:28, 11 March 2025
  • Thumbnail for Complete blood count
    sickle cell anemia and thalassemia. The reference ranges for the complete blood count represent the range of results found in 95% of apparently healthy people...
    106 KB (12,446 words) - 06:39, 6 April 2025
  • promote proper red blood cell shape reducing the effects of sickle cell disease. Beta thalassemia is a heritable disorder, characterized by the inability...
    11 KB (1,227 words) - 00:53, 27 May 2025