These findings are similar to those commonly noted in hereditary spherocytosis and do not conform to either the Type 1 or the Type 2 pattern of congenital nonspherocytic hemolytic anemia.

Hereditary spherocytosis (HS) is a genetic condition that leads to hemolytic anemia, a disorder where red blood cells are destroyed faster than they can be made. This condition is characterized by ...

Hemolytic anemia may lead to an MCHC measurement above ... Higher-than-normal MCHC results may also be attributable to hereditary spherocytosis, a rare genetic condition in which the body makes ...

In pregnancies at risk of hemolytic disease of the fetus and newborn (HDFN), amniocentesis is used to identify the fetus’s ...

The direct antiglobulin test was positive for anti-C3d specificity, with cold agglutinin titer confirming the diagnosis of CAD.

In Guangxi, Hainan, and Fujian Province in southern China, β-thalassemia is a frequent monogenic hereditary disorder that is primarily defined by hemolytic anemia brought on by inefficient ...

Expresses differences in erythrocyte size in an individual specimen Used to detect anisocytosis. Increased in immune hemolytic anemia, SS and SC disease, and hereditary spherocytosis ...

Jennison Associates LLC lifted its position in shares of Rocket Pharmaceuticals, Inc. (NASDAQ:RCKT – Free Report) by 72.6% during the 4th quarter, according to its most recent filing with the ...

SG Americas Securities LLC grew its stake in Rocket Pharmaceuticals, Inc. (NASDAQ:RCKT – Free Report) by 796.2% in the 4th quarter, Holdings Channel.com reports. The firm owned 54,921 shares of the ...

These disorders can be inherited ... Anemias: Hemolytic anemias are a group of disorders characterized by the premature destruction of red blood cells, leading to anemia. Treatment depends on ...

"For any case of inbreeding of a Neanderthal female with a Homo sapiens or Denisova male," Mazières said, "there is a high risk of hemolytic disease of the newborn." The condition can lead to jaundice ...