WebMar 22, 2024 · Hereditary spherocytosis (HS) is a familial hemolytic disorder associated with a variety of mutations that lead to defects in red blood cell (RBC) membrane proteins. The morphologic hallmark of HS is the microspherocyte, which is caused by loss of RBC membrane surface area and has abnormal osmotic fragility in vitro. WebHereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells , yellowing of the eyes and skin (jaundice), and an enlarged spleen …

2024 ICD-10-CM Diagnosis Code D58.0: Hereditary spherocytosis

WebFamilial adenomatous polyposis (FAP) is an autosomal dominant inherited condition in which numerous adenomatous polyps form mainly in the epithelium of the large intestine.While these polyps start out benign, … WebHereditary spherocytosis (HS) is a congenital hemolytic disorder, wherein a genetic mutation coding for a structural membrane protein phenotype leads to a spherical shaping of erythrocytic cellular morphology. As … honeycott inc

Previously undiagnosed hereditary spherocytosis in a patient …

WebHereditary spherocytosis refers to a group of heterogeneous disorders that are characterized by the presence of spherical-shaped erythrocytes (spherocytes) on the peripheral blood smear. The disorders are characterized clinically by anemia, jaundice, and splenomegaly, with variable severity. Common complications include cholelithiasis, … WebNov 15, 2024 · Although relatively rare, hereditary spherocytosis (HS) is the most common cause of hemolytic anemia due to a red cell membrane defect. It is a result of … WebEzra, age 6, suffers from a rare hereditary disease, spherocytosis, which leads to severe anemia. When Ezra was born, his parents were told he had less than... honey cottage caravan park ettrick