Google
Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Sickle Cell Disease: Aplastic Crisis
source: Healthwise
year: 2017
summary/abstract:If a person with sickle cell disease is infected with parvovirus, the virus that causes fifth disease in children, an aplastic crisis may develop. Bone marrow suddenly stops producing red blood cells, which results in sudden and severe anemia. During this time, a person will often feel tired, have pale skin, and be short of breath.
Blood transfusions might be done to treat an aplastic crisis. After a few days, the bone marrow usually recovers on its own. And red blood cell production returns to its usual rate.
Most aplastic crises occur in children. This condition only occurs once in any person.
read more
+myBinderRelated Content
-
Sickle Cell Retinopathyhttps://www.youtube.com/watch?v=tCgAHWvV...
-
A Developmental Examination of Pain Among Youth with Sickle Cell DiseaseIntroduction: Sickle cell disease (SCD)...
-
Living With Sickle Cell Disease Is a Constant Battle With Pain, According to one Woman Who Has It“You don’t look sick.” That’s ...
-
Sickle cell trait may not increase the risk of deathPeople who carry a gene for sickle cell ...
-
Phase 1 trial to test under-the-skin injection of sevuparin in sickle cell patientsModus Therapeutics is going to launch ...
-
Treatment for avascular necrosis of bone in people with sickle cell diseaseBACKGROUND: Avascular necrosis of bone ...
-
New Guidelines for Managing Sickle Cell Disease Presented at ACP Internal Medicine MeetingNew guidelines for therapeutic strategie...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.