Genetic Disorders

Genetic Disorders in Humans
There are thousands of genetic disorders in humans. Some are common whereas quite a few are rare. Whatever be their incidence, what is most vexing about these disorders is that scientists are still trying to find cures for these disorders. While some headway has been made in the direction, a lot more research is required. Here is a comprehensive view of genetics and various genetic disorders in humans.

Spinocerebellar Ataxia: Symptoms and Treatment
Spinocerebellar ataxia is a degenerative genetic disease. It has many forms, each of them, being so vast and complex, can be coined as diseases themselves. Read on to know all about it.

Friedreich's Ataxia: Symptoms and Treatment
Friedreich's ataxia is an inherited disease, that causes a failure in muscle coordination which results in an unsteady gait and imbalance of limb or eye movements, and abnormal speech. To know more about Friedreich's ataxia, its symptoms and treatment, read on.

Crouzon Syndrome
Crouzon syndrome is a genetic disorder resulting in the distortion of the shape of the head and face. This disorder affecting nearly 16 million people is caused by the fusion of the skull bones, leading to abnormal growth of the skull.

Hereditary Angioedema
Hereditary angioedema is a type of angioedema caused due to the deficiency of a blood protein, C1 inhibitor. To know the causes, symptoms and treatment for hereditary angioedema, read on...

Facts about Cystic Fibrosis
Cystic Fibrosis is a degenerative disease of a persons secretory glands, that affects many of the body functions, including respiration, digestion and reproduction.

Interesting Facts about Fragile X Syndrome
Fragile X syndrome is named so as the chromosome with the mutated gene appears as if it will break down. The symptoms of this syndrome are more severe in boys as compared to girls. Read on to know more about the facts of fragile X syndrome.

Neurofibromatosis: Causes, Symptoms and Treatment
Neurofibromatosis is a genetic disorder of the nervous system which mainly affects the development and growth of neural cell tissues. What are the causes, symptoms and treatment of neurofibromatosis? To know more, read on...

Beneficial Mutation
Mutation, a change in the gene sequence, is divided into beneficial, harmful and neutral, based on the effects. To know more about beneficial mutation, read on...

Causes and Symptoms of Klinefelter Syndrome
Klinefelter Syndrome is a genetic sex disorder that occurs due to an error during sex cell division. Klinefelter Syndrome occurs when, instead of 46 chromosomes in the human cell, a total of 47 are present, wherein the extra chromosome is an X chromosome. The chromosomal pattern is XXY and is only seen in men.

Centronuclear Myopathy - Symptoms, Causes and Treatments
Centronuclear myopathy is a genetic disorder and it involves muscle tissues related problems and centrally positioned nuclei of muscle cells.

Canavan Disease - Symptoms, Causes and Treatments
Canavan disease is a genetic disorder caused due to mutation in gene that helps in production of Aspartoacylase enzyme.

Aicardi Syndrome - Causes, Symptoms and Treatment
Aicardi syndrome is a genetic disorder caused due to gene mutations and is mainly found in females. The male version of this disorder is very rare and lethal.

Facts about Huntington's Disease
Huntington's disease is a hereditary disorder of the brain, caused by the degeneration of certain nerve cells. Read on to understand the facts about Huntington's disease.

Prader-Willi Syndrome - Causes, Symptoms and Treatment
Prader-Willi syndrome is a rarely occurring genetic disorder caused due to deletion of genes/regions on chromosome 15.

Fragile X Syndrome - Symptoms, Causes and Treatment
Fragile X syndrome is a genetic disorder related to behavioral, intellectual, emotional and physical characteristics of a person and is a result of gene mutation. Read on...

Alexander Disease - Symptoms, Causes and Treatment
Alexander disease is a rare genetic disorder of the nervous system. To know more about the symptoms, causes and treatment of Alexander disease, read on...

Facts about Albinism
People with albinism usually have light color skin and hair, with impaired vision. However, the skin and hair color of each individual with albinism vary, depending upon the amount of pigment present. Here are some facts about albinism.

Rare Genetic Diseases and Disorders
Genetic diseases are caused due to disorder in the genome of an individual. They result in many chronic conditions that have no cure; however, researches on treatment for rare genetic diseases and disorders are ongoing.

Inherited Genetic Diseases
What is a genetic disease? How are genetic disorders inherited? Read on to find the answers.

Spinal Muscular Atrophy - SMA
Spinal Muscular Atrophy, SMA for short, is a genetically transmitted disease, which can result in the progressive weakening and degeneration of muscles. Read more about it here.

Klinefelter Syndrome
Read on to know more about Klinefelter Syndrome, its symptoms and its causes…

Genetic Diseases: List of Genetic Disorders
Genetic Diseases, often known as heridatory diseases are caused due to abnormalities in genes.Let us have a look at the few of them in this List of Genetic Diseases...

Bowel Cancer - A Genetic Disease
This article discusses about the genetic disease, bowel cancer and the symptoms of this genetic disease in brief. The article further discusses about the prevention of this genetic disease.

Genetics and Personality Disorders
To identify the role of heredity, researchers have resorted to a few tactics: they studied the occurrence of similar psychopathologies in identical twins separated at birth, in twins and siblings who grew up in the same environment, and in relatives of patients (usually across a few generations of an extended family).

Our Genes are Not Our Fate
While genes are undeniably important factors in causing disease, their role has been vastly overemphasized. For most common diseases, such as cancer and atherosclerosis, genes are predispositions, not inevitabilities.