Hereditary OvalocytosisSymptoms, Doctors, Treatments, Advances & More
Hereditary Ovalocytosis Overview
Learn About Hereditary Ovalocytosis
Hereditary ovalocytosis is a rare condition passed down through families (inherited). The blood cells are oval-shaped instead of round. It is a form of hereditary elliptocytosis.
Ovalocytosis - hereditary
Hereditary ovalocytosis is mainly found in Southeast Asian populations.
Newborn infants with hereditary ovalocytosis may have anemia and jaundice. Adults most often do not show symptoms.
In severe cases, the disease may be treated by removal of the spleen (splenectomy).
Elena Krishnevskaya practices in Badalona, Spain. Ms. Krishnevskaya is rated as an Elite expert by MediFind in the treatment of Hereditary Ovalocytosis. Her top areas of expertise are Hereditary Elliptocytosis, Hereditary Ovalocytosis, Hereditary Spherocytosis, and Anemia.
Tennessee Cancer Specialists
. Dr. Tumkur is rated as an Experienced provider by MediFind in the treatment of Hereditary Ovalocytosis. His top areas of expertise are Familial Colorectal Cancer, Colorectal Cancer, Acute Mountain Sickness, and Anemia.
Saint Vincent Medical Group-Eaton Place Oncology
Archana Agarwal is a Hematologist and an Oncologist in Worcester, Massachusetts. Dr. Agarwal is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ovalocytosis. Her top areas of expertise are Hereditary Pyropoikilocytosis, Hereditary Spherocytosis, Hereditary Elliptocytosis, Hereditary Ovalocytosis, and Splenectomy.
The condition may be associated with gallstones or kidney problems.
Published Date: March 31, 2024
Published By: Todd Gersten, MD, Hematology/Oncology, Florida Cancer Specialists & Research Institute, Wellington, FL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
Gallagher PG. Hemolytic anemias: red blood cell membrane and metabolic defects. In: Goldman L, Cooney KA, eds. Goldman-Cecil Medicine. 27th ed. Philadelphia, PA: Elsevier; 2024:chap 147.
Gallagher PG. Red blood cell membrane disorders. In: Hoffman R, Benz EJ, Silberstein LE, et al, eds. Hematology: Basic Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2018:chap 46.
Prozora S, Gallagher PG. Hereditary elliptocytosis, hereditary pyropoikilocytosis, and related disorders. In: Kliegman RM, St. Geme JW, Blum NJ, et al, eds. Nelson Textbook of Pediatrics. 22nd ed. Philadelphia, PA: Elsevier; 2025:chap 508.