Literature DB >> 32548653

[Sickle cell disease].

L Distelmaier1,2, U Dührsen3, R Dickerhoff4.   

Abstract

The term "sickle cell disease" covers a group of genetic blood disorders caused by sickle hemoglobin (HbS) alone or in combination with other variants of the β‑globin locus. Sickle cell disease occurs frequently in sub-Saharan Africa, but is also common in Turkey, Greece, Sicily, the Middle East, India, and the Americas. Polymerization of deoxygenated sickle hemoglobin leads to decreased deformability of red blood cells. These altered erythrocytes can obstruct small blood vessels and cause acute episodes of pain, hemolytic anemia, and organ damage. Complications can vary between the different genotypes and it is important to be aware of the special features of the disease. Hydroxycarbamide has been shown to reduce the morbidity and mortality of patients with sickle cell disease. New drugs and novel treatment approaches such as gene therapy are currently being tested.

Entities:  

Keywords:  Acute chest syndrome; Genetic therapy; Hemoglobin, sickle; Hydroxycarbamide; β‑Globins

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Year:  2020        PMID: 32548653     DOI: 10.1007/s00108-020-00822-z

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  1 in total

1.  Transcranial Doppler sonography and the effect of haematopoietic stem cell transplantation in sickle cell disease.

Authors:  Sylvia Thurn; Katharina Kleinschmidt; Irena Kovacic; Christina Wendl; Ralf A Linker; Selim Corbacioglu; Felix Schlachetzki
Journal:  Neurol Res Pract       Date:  2022-04-04
  1 in total

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