Sickle Cell Disease

Sickle cell disease (SCD) is a red blood cell disease, a complex inherited disorder with multisystem manifestations that requires specialized comprehensive care to achieve an optimal outcome. Appropriate treatment requires the active involvement of health care professionals with expertise in the management and treatment of SCD working in c with a multidisciplinary team,  a ‘Medical Home’. The most appropriate medical home is a multidisciplinary sickle cell clinic that coordinates all aspects of comprehensive care in collaboration with the primary care providers. In other cases, the medical home may be provided by a knowledgeable primary care provider or other health care professional from whom patients receive day-to-day care, with periodic referrals to sickle cell specialists for comprehensive evaluations and for the management and treatment of severe, life-threatening complications.

Last modified
7 May 2020
OMIM

# 603903 SICKLE CELL ANEMIA

ORPHA

ORPHA 232

Patient Organization

June 2017 Sororya Beacher, Oscar Netherlands

As chairman of the sickle cell organization in the Netherlands, a trained ICU nurse, and nurse tutor this has given...

General Medical Guideline
Sickle Cell Disease (SCD) is a genetic disorder caused by homozygosity for a single β-globin gene mutation (β6GAG → GTG), in which glutamic acid has...
Disease
Symptom
When sickle cell disease is suspected by the HPLC pattern usually additional tests are performed to confirm the diagnosis. Ultimately it would be best to...
Anemia can be the first feature of sickle cell disease and thalassemia when the disease manifests from about the age of 6 months. This happens...
Acute pain in extremities, the back, or the belly is caused by vascular occlusion in the blood vessels of the bone or gut. Children with...