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v. sick·led, sick·ling, sick·les
To deform (a red blood cell) into an abnormal crescent shape.
To assume an abnormal crescent shape. Used of red blood cells.
Shaped like the blade of a sickle; crescent-shaped: a sickle moon.

Patient discussion about sickle

Q. Please precribe for me the possible medicine (treatment) for sickle cells. Secondly, my boy lost hearing at 4 1- I need to know how sickle cells can be treated. 2- My boy just surprisingly lost his abillity to hear anything at the age of 4.

A. are going through some hard's the hardest thing in the world seeing your children in pain. loosing his hearing could be caused by clots that were formed and destroyed the ear nerve. but it's unlikely it happened in both i would check it out. and about treatment- there are a variety of treatments, so i found a web site with them all. and even some that are still in research:

More discussions about sickle
References in periodicals archive ?
Patients who were treated with Xyndari over a 48-week period experienced fewer crisis episodes compared to patients who received a placebo, fewer hospitalizations for sickle cell pain, and fewer days in the hospital.
Biree Andemariam, director of the New England Sickle Cell Institute at the University of Connecticut Health Center, has talked to her adult patients about CRISPR's potential for treating sickle-cell disease.
Senator Scott hopes this resolution will continue to amplify the seriousness of Sickle Cell Disease while pushing for people across the country to highlight the urgency of finding a widely accessible cure, identifying early detection methods, and ensuring living with the disease are aware of available resources.
To assess the changes in right ventricle in patients of sickle cell anaemia using echocardiographic estimates of systolic function, pressure, size and RV free wall mass.
I have started attending different majlises and posted several messages online urging sickle cell patients in Bahrain not to fast during Ramadan," said Mr Al Kadhem.
The researchers have designed and are using gene editing tools to correct the sickle hemoglobin mutation using the stem cell lines.
Sickle cell disease (SCD) is an inherited blood disorder caused by a genetic mutation in the beta-chain of hemoglobin, leading to formation of abnormal hemoglobin known as sickle hemoglobin, or HbS.
While the mortality rate for sickle cell disease in children decreased 3 percent each year in a study from 1979 to 2005, the mortality rate for adults with the disease increased by 1 percent each year.
Al-Mutawa commended the role played by the Bahrain Society for Sickle Cell Anaemia Patient Care in taking care of the affairs of the sickle cell patients and informing the community about the disease, as well as about ways to prevent it and limit its spread.
Population estimates of sickle cell disease in the U.
Renal disease is a known complication of sickle cell disease.
This prospective single centered case control study was conducted at the department of Pediatrics and Biochemistry and sickle cell research centre at a tertiary care centre (VSS Medical College, Burla, Sambalpur) over a period of 1year ending in July 2012.