Hemoglobin SS Disease

Hemoglobin SS disease, one of the forms of sickle cell anemia, is an inherited disorder in which the red blood cells take on a sickle shape that makes it hard for them to circulate through the blood vessels.

Common causes: It is caused by a genetic alteration inherited from both parents that changes hemoglobin, the protein responsible for carrying oxygen in the blood.

Frequent symptoms: Fatigue from anemia, episodes of intense pain in the bones and joints, paleness, a greater tendency to infections, and swelling of the hands or feet.

Which specialist treats it? The hematologist is the professional who studies and supports those living with this condition. If there is a family history or episodes of unexplained pain and anemia, an evaluation with this specialist is advisable.