A series of genetic red blood cell disorders known as sickle cell disease results in cells that are crescent-shaped rather than disk-shaped. The protein haemoglobin, which transports oxygen throughout the body, has been linked to anomalies.
A plan for managing disease symptoms is essential to improving patient outcome and necessitates close coordination with healthcare professionals. Patients with the disease are now living longer than they did in the past thanks to an improved understanding of how the disease operates and earlier Sickle Cell Anemia Therapeutics diagnosis and treatment. When patients switch from seeing a paediatrician to an adult-focused physician, this partnership is extremely crucial.
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