This section has a list of generic name(s) and the several brand name(s) of the drugs used for the treatment of
Diseases - Genetic Testing (Genetic Testing of Diseases ). Its purpose is to provide doctors and consumers a ready reckoner to find the relevant drugs.
The information helps you learn more about the generic drug, including its brand name(s), price, dosage, side effects, adverse events, how to take and appropriate times to take it by simply click on the drugs. Plus there are FAQs too about each drug.
Recommended Readings
Achondroplasia is a rare genetic disorder of bone growth that causes short-limbed dwarfism. It occurs due to mutations in a single gene called the FGFR3.
Alzheimer''s disease is a progressive neurodegenerative disease affecting memory and thinking and making the person increasingly dependent on others.
The crab that invades the breast is no more a fear factor with all the advancements that medical science and customized protocols can fight breast cancer. the recent developments in the management of breast cancer.
Cervical cancer is the second most common cancer among women and is the primary cause of cancer-related deaths in developing countries
DNA fingerprinting is a technique which helps forensic scientists and legal experts solve crimes, identity thefts, legal suits and terrorism cases.
Achondroplasia is a genetic disorder which is one of the leading causes of dwarfism
Overview about muscular dystrophy, a muscle disease characterized by muscle weakness and muscle wasting.
'Paa' is a film in which Amitabh Bachchan, in a rare role reversal, plays son to Abhishek Bachchan, his real-life son!
Von Recklinghausen's Disease / Neurofibromatosis can cause bone deformities and skin problems. Multiple soft-nerve tumors or neurofibromas are seen. Light brown tan spots develop on the skin.
Ionizing radiation can damage living tissue in the human body. It strips away electrons from atoms breaks some chemical bonds.
Tuberous sclerosis is genetic disorder characterized by benign tumors in many parts of the body, including brain, skin, lungs, kidney and heart.
Porphyria or vampire disease or is a group of inherited diseases that cause symptoms of the nervous system and/or skin. Treatment depends on the type of porphyria.
Christianson syndrome is a condition that occurs due to mutations (abnormal changes) in the gene SLC9A6 that is present on X chromosome. It primarily affects the nervous system.
Seckel syndrome is a rare genetic disorder characterized by an abnormally small head, birdlike facial features, mental retardation, and blood malignancies.
Aicardi-Goutieres Syndrome is observed in infants and older children. To date, defects in 6 genes are known to cause the syndrome. Irritability, erratic sleep, and fever are some symptoms.
Williams syndrome is a rare genetic disorder due to a deletion in the long arm of chromosome 7.
Alagille syndrome is a rare genetic disorder that is caused by hereditary or spontaneous mutations in JAG1 or NOTCH2 on chromosome 20. Liver damage is a prominent symptom of this condition.
Galactosemia is one of many genetically inherited diseases and it affects one's ability to process galactose. Learn about the symptoms, diagnosis and treatment for galactosemia.
Find the facts of coffin-Lowry syndrome including Symptoms, Causes, Treatment, Diagnosis, Prevention and more information.
Noonan syndrome is a genetic disorder that affects different parts of the body. It is caused by changes in one of various autosomal dominant genes.
Huntington's disease is a genetic degenerative disorder that affects the brain and causes psychiatric, motor and cognitive dysfunction. Learn about causes, symptoms and treatment
Mucopolysaccharidosis (MPS) are a group of inborn metabolic disorders due to the absence or malfunctioning of specific enzymes required to process molecules called glycosaminoglycans.
Ever wondered how your intelligence level is different from others? learn more about how genetic makeup can guide intelligence during your lifespan
Rare or orphan diseases are least understood of all chronic diseases. They are more common than projected and kill more people than cancer and HIV together.
Harlequin ichthyosis or ichthyosis congenita is a genetic disorder that results in a thick, dry and scaly skin with fissures and is often fatal.
Turner syndrome, a genetic developmental disorder in females is caused by a missing or incomplete X- chromosome. Girls are short and have dysfunctional ovaries.
Incurable diseases are disorders of infectious, non-infectious, genetic, metabolic, neoplastic or autoimmune nature that do not currently have a cure.
Apert syndrome is a rare inherited condition marked by abnormal shape of the face and skull due to premature fusion of the bones, and webbing of hands and feet.
Hunter Syndrome is a rare inherited disease in which the breakdown of sugars that build connective tissues is impaired due to the malfunctioning of an enzyme.
Muir-Torre syndrome is a subtype of Lynch syndrome or HNPCC. It is a rare autosomal dominant cancer syndrome, characterized by neoplasms of the sebaceous glands and visceral organs, especially colon cancer.
Gene Therapy - Potential Treatment for Incurable Diseases Gene therapy is a novel procedure in which genetic material is introduced into a patient's cells to replace a faulty gene in order to try and cure disease. It holds promise in ...
