Genetic modulation of stroke in children with sickle cell anaemia

Sickle cell anaemia (SCA) is an autosomal recessive genetic disease that leads to the synthesis of haemoglobin S (HbS). The pathophysiology of the disease is centred on HbS polymerization inside the red blood cells, which become sickle-shaped (SSRBCs), rigid, viscous and adherent-prone to the vascul...

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Bibliographic Details
Main Author: Silva, Marisa (author)
Other Authors: Vargas, Sofia (author), Coelho, Andreia (author), Mendonça, Joana (author), Vieira, Luís (author), Kjollerstrom, Paula (author), Maia, Raquel (author), Silva, Rita (author), Dias, Alexandra (author), Ferreira, Teresa (author), Morais, Anabela (author), Mota Soares, Isabel (author), Lavinha, João (author), Faustino, Paula (author)
Format: conferenceObject
Language:eng
Published: 2020
Subjects:
Sickle Cell Anaemia
Drepanocitose
Anemia das Células Falciformes
Hemoglobinopatias
AVC
Modificadores Genéticos
Vasculopatia cerebral
Medicina Personalizada
Doenças Genéticas
Doenças Raras
Genética Humana
Online Access:http://hdl.handle.net/10400.18/6811
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/6811

Internet

http://hdl.handle.net/10400.18/6811

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