What is another word for hereditary stomatocytosis?
Pronunciation: [hɪɹˈɛdɪtəɹi stəmˌɑːtəsɪtˈə͡ʊsɪs] (IPA) 
Hereditary stomatocytosis, also known as familial hemolytic anemia or hereditary ellipse-shaped red blood cells, is a rare genetic disorder that affects the red blood cells' shape and function. The condition is caused by mutations in genes that control the flow of ions across the cell membrane. Symptoms may include fatigue, anemia, jaundice, and an enlarged spleen. For the condition, several synonyms are used such as hereditary spherocytosis, stomatocytic hemolytic anemia, and hereditary pyropoikilocytosis. Treatment for hereditary stomatocytosis is generally supportive and may include transfusions, splenectomy, and iron supplements. Genetic counseling may also be recommended for families with a history of the condition.
