https://elioacademy.org/student/23/kirthi-gopinath
Congenital Heart Defects (CDHs) are present at birth and affect the structure of a baby's heart as well as its function. One specific CDH, Atrial Septal Defect (ASD), causes a hole to form in the septum that divides the right and left atria. This hole causes irregular blood flow by allowing blood from the left atrium to flow to the right atrium
https://elioacademy.org/student/23/jerry-lou
Tay-Sachs disease is a relatively rare genetic disorder where it is passed down from parents to offspring. According to the Mayo Clinic, Tay-Sachs disease occurs when there is an absence of an enzyme, Hex A(Beta-Hexosaminidase A), which helps with breaking down fatty substances called gangliosides.This accumulation of gangliosides results in build up of toxic levels in the brain and spinal cord and affect the function of nerve cells.
https://elioacademy.org/student/23/margarita-cham-beatrice-fernandez
Hemophilia A is a disorder characterized by a deficiency of the protein "clotting Factor VIII" in the bloodstream. This deficiency leads to prolonged bleeding following injuries such as tooth extractions, surgeries, and delayed or recurring bleeding during the wound-healing process. Hemophilia A is categorized into three main levels of severity: severe, moderate, and mild.
https://elioacademy.org/student/jaein-kho-22
Cystic Fibrosis is a genetic disorder that is caused by a mutation in the Cystic fibrosis transmembrane conductance regulator ( CFTR ) gene. Cystic Fibrosis is an autosomal recessive disorder; therefore in order for a patient to have CF, the patient has to have acquired at least one mutated CFTR gene from each parent whether homozygous or heterozygous.