Hereditary oral hypercytosis in children
Hereditary stomatocytosis (HST) is a rare autosomal dominant hereditary hemolytic disease, characterized by a marked increase in the number of oral cells in the blood and exceeding 5%. Clinically, there is often moderate to severe hemolytic anemia. Peripheral blood smears show a clear-shaped mouth-shaped fissure in the lightly stained area of the center of the red blood cells, which has a mortar or mortar shape under the scanning electron microscope.
The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.