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Hemangiomas
This Helping Hand™ explains different types of hemangiomas and how they're benign (noncancerous).
Learn MoreHemifacial Microsomia (HFM) in Children
Hemifacial microsomia (HFM) is a congenital disorder. This means that your child is born with it. In this condition, one side of your baby’s face is underdeveloped (hemi means half). HFM usually only affects one side of the face. Sometimes both sides may be affected.
Learn MoreHemoglobin C Disease
Most people carry hemoglobin A in their red blood cells. Those who carry hemoglobin C, considered an abnormal variation, may develop hemoglobin C disease. This blood disorder develops because the red blood cells break down earlier than they should, leaving too few in the blood and leading to mild anemia.
Learn MoreHemoglobin E Trait
Hemoglobin E trait is an inherited blood disorder. That means it's passed down through your parent’s genes. Read on to learn more.
Learn MoreHemoglobinopathy
Learn MoreHemolytic Anemia in Children
Hemolytic anemia is a group of disorders in which the red blood cells are destroyed faster than the bone marrow can make them. Learn more about the causes, symptoms, diagnosis, and treatment.
Learn MoreHemolytic Disease of the Fetus and Newborn (HDFN)
Hemolytic disease of the fetus and newborn (HDFN) is a blood disorder that causes a baby’s red blood cells to break down quickly (hemolysis). HDFN occurs when there is a mismatch between the mother’s and baby’s blood type and/or Rh factor during pregnancy. Hemolysis causes anemia and jaundice.
Learn MoreHemolytic Disease of the Newborn (HDN)
Hemolytic disease of the newborn (HDN) is a blood problem in newborns. It occurs when your baby's red blood cells break down at a fast rate. It’s also called erythroblastosis fetalis.
Learn MoreHemolytic Uremic Syndrome in Children
Hemolytic uremic syndrome (HUS) is a rare condition that can lead to kidney failure. The syndrome harms the small structures and vessels inside the kidneys. HUS causes red blood cells to clog the tiny blood vessels in the kidneys. It may cause damage to the kidney tissues.
Learn MoreHemophilia
Hemophilia is an inherited bleeding disorder. People with hemophilia can’t stop bleeding because they don’t have enough clotting factor in their blood. Clotting factors are needed for blood to clot. Blood clots to prevent excessive bleeding.
Learn MoreHemophilia
Hemophilia is an inherited blood disorder. In hemophilia, a blood clotting factor is missing. In Hemophilia A, Factor VIII (8) is missing. In Hemophilia B, Factor IX (9) is missing. Without these factors, blood will not clot well. People with hemophilia are born with the disorder. It is not contagious.
Learn MoreHemophilia Carrier
A hemophilia carrier is a female who has the gene that causes hemophilia A or hemophilia B deficiency.
Learn More
Helping Hands Patient Education Materials
Written and illustrated by medical, nursing and allied health professionals at Nationwide Children's Hospital, Helping Hand instructions are intended as a supplement to verbal instructions provided by a medical professional. The information is periodically reviewed and revised to reflect our current practice. However, Nationwide Children's Hospital is not responsible for any consequences resulting from the use or misuse of the information in the Helping Hands.