Introduction
Healthcare providers prescribe NIPT tests, to pregnant women to evaluate the risk of certain genetic conditions in the fetus. The test assesses genetic diseases and predispositions during the fetal development stage.
NIPT is a safe method of screening genetic…
Introduction Leber Hereditary Optic Neuropathy (LHON) is a rare mitochondrial disorder that primarily affects the optic nerves, leading to progressive vision loss. Named after the German ophthalmologist Theodor Leber, who first described it in the 19th century, LHON typically manifests in young…
Hereditary Angioedema (HAE) is a rare genetic disorder that causes recurrent episodes of severe swelling, or angioedema, in various parts of the body. The symptoms of Hereditary Angioedema can be unpredictable and debilitating. Unlike common allergic reactions, Hereditary Angioedema does not respond…
Introduction Hereditary Spherocytosis (HS) is an inherited blood disorder characterized by the presence of spherocytes—abnormally shaped red blood cells (RBCs) that are sphere-shaped instead of the typical biconcave disc shape. Recognizing Hereditary Spherocytosis symptoms is crucial for an accurate Hereditary Spherocytosis diagnosis.…
Understanding The Concept Of Heredity Hereditary is passed on from parent to child in the form of genes, sperm, or eggs. Hereditary are the traits and conditions passed on from one generation that can be positive and negative. The term hereditary emphasizes…
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu Disease, is a rare genetic condition that affects blood vessels. The disorder contributes to the formation of abnormal blood vessels. As a result, vascular function gets impaired. This condition gives rise to various symptoms…