Catalog

Sickle cell Hb-C disease with crisis with splenic sequestration

No MMS code

Link to WHO Definition

Sickle cell Hb-C disease with crisis with splenic sequestration – http://id.who.int/icd/entity/581104423

A disease caused by the inheritance of a HbS mutation from one parent and a HbC mutation from the other parent. This disease is characterised by abnormal rigid sickle-shaped red blood cells, crisis, and splenic sequestration. This disease may present with enlargement of spleen, fatigue, shortness of breath, acute chest pain, coughing, dizziness, headaches, pallor of skin or mucous membranes, hypoxia, fever and jaundice. This disease is confirmed by identification of HbS and HbC mutation by genetic testing.