^

Health

A
A
A

Thalassemia HbS-B: Causes, Symptoms, Diagnosis, Treatment

 
, medical expert
Last reviewed: 18.10.2021
 
Fact-checked
х

All iLive content is medically reviewed or fact checked to ensure as much factual accuracy as possible.

We have strict sourcing guidelines and only link to reputable media sites, academic research institutions and, whenever possible, medically peer reviewed studies. Note that the numbers in parentheses ([1], [2], etc.) are clickable links to these studies.

If you feel that any of our content is inaccurate, out-of-date, or otherwise questionable, please select it and press Ctrl + Enter.

Thalassemia HbS-B is hemoglobinopathy, in which the symptoms are similar to sickle-cell anemia, but less pronounced.

Because of the high incidence of thalassemia HbS and beta-thalassemia in certain population groups, the congenital presence of both anomalies is quite frequent. Clinically, the disease manifests itself as symptoms of mild anemia and signs of sickle-cell anemia, which are usually more rare and less intense. In blood smears, in most cases, mild to moderate severity of microcytic anemia with some sickle-shaped erythrocytes occurs. To establish the diagnosis, you need a quantitative determination of hemoglobin, the level of HbA 2 > 3%. Electrophoresis determines the increase in HbS and the decrease or absence of HbA, there may be an increase in HbF. Treatment, if necessary, is similar to that of sickle cell anemia.

You are reporting a typo in the following text:
Simply click the "Send typo report" button to complete the report. You can also include a comment.