Genes play an important part in a person's characteristics and health conditions. Some genetic changes that are responsible for causing a medical syndrome or condition can be passed down from the parents to the baby. These are often caused by genetic mutations in single or multiple genes, chromosomal damage, and environmental factors affecting the genes. These genetic diseases or disorders that are inherited from the parents making the offspring more susceptible or born with the condition, are known as inherited diseases.
Inherited Thrombocytopenia
Inherited thrombocytopenia refers to a group of genetic disorders characterized by low platelet counts, leading to increased bleeding tendencies.
Inherited Periodic Fever Syndrome: Recurrent Fever and More
Inherited periodic fever syndromes are a group of diseases marked by recurrent episodes of fever with inflammatory symptoms.
Polycystic Kidney Disease - Causes, Symptoms, Diagnosis, and Management
Polycystic kidney disease is a genetic condition indicated by the formation of multiple cysts in the kidney. To know more, read the article below.
Renal Cystic Abnormalities in Inherited Diseases - An Overview
A collection of pathologic diseases linked to the development of renal cysts is referred to as renal cystic disease (RCD).
Focal Spinal Muscular Atrophy - Causes, Diagnosis and Treatment
Spinal muscular atrophy is an inherited disease that weakens the muscles and nerves. Read the article to know more.
Tricho-Rhino-Phalangeal Syndrome Type 2
Tricho-rhino-phalangeal syndrome type 2 is an extremely rare condition affecting multiple systems of the body. Read further to know more about this condition.
Pendred Syndrome - An Overview
Pendred syndrome is a disorder that is associated with hearing loss and certain thyroid conditions. Read below to know more in detail.
Primary Deficiencies of Complement Components - Types, Symptoms, Diagnosis, and Treatment
Primary deficiencies of complement components lead to reduced immunity in the body. Read below to learn about the same.
Cerebrotendinous Xanthomatosis- Causes, Symptoms, Diagnosis, and Management
Cerebrotendinous xanthomatosis is a condition affecting the fat metabolism of the body. This article reviews cerebrotendinous xanthomatosis and its management.
