Genetic Disorders

Passed on from generations to generations, genetic disorders are an effect of faulty genes and chromosomes. Read on to know more about how to deal with genetic ailments.
  • Lesch-Nyhan Syndrome Symptoms
    Lesch-Nyhan Syndrome or Lesch-Nyhan Disease is a rare genetic disorder occurring with both physiological as well as behavioral symptoms. Let us broaden our understanding of this uncommon illness by examining its symptoms and exploring available treatment options.
  • Autosomal Dominant Genetic Disorder
    Autosomal dominant genetic disorder is a genetic condition where just a single copy of mutant allele is required to express the defect in the progeny. The following article will explain more about the inheritance this genetic disease.
  • Recessive Genetic Disorders
    Autosomal recessive genetic disorders are those that requires a pair of mutated genes to express certain diseases. Some of the recessive genetic disorders in humans are explained in the following article. Read on to know more...
  • Genetic Brain Disorders
    Illnesses that affect the brain have adverse effects on nearly all parts of the body. Normal functioning of an individual, both physically and mentally is severely compromised due to the disease's far-reaching impact. If such disorders are hereditary, the risk of contraction and complications are doubled. Scroll below to learn which brain disorders are hereditary in nature.
  • Rare Genetic Skin Disorders
    There are many rare genetic skin disorders that affect the appearance of the skin. Some of these rare genetic skin diseases are covered in the following article. Read on, to know more about these rare skin conditions.
  • Huntington's Disease Treatment
    Huntington's disease treatment options include drug therapy, psychotherapy, speech therapy, etc. Scroll down to find out more about the causes, symptoms and treatment of Huntington's disease.
  • Treatment of Hereditary Diseases
    Hereditary diseases are passed down from one generation to the succeeding generation(s) through genes. A lot of research and development has been done with regards to treatment of hereditary diseases that deserves some attention. Read ahead to get acquainted with some intriguing facts related to this subject.
  • Most Common Genetic Diseases
    Genetic diseases are those which result from abnormalities present in the genes. This article presents information about the most common genetic diseases that affect human beings.
  • Huntington's Disease Symptoms
    Changes in behavior and memory are some of the common Huntington's disease symptoms. In this article you will find causes, symptoms, and treatment of Huntington's disease.
  • Hurler's Syndrome
    Some genetic disorders that affect children are rare and have serious complications. Learn more about one such disorder, Hurler's syndrome, and its signs.
  • Genetic Disorders in Babies
    Genetic disorders in babies is caused by a glitch in the DNA. Addition, subtraction or mutation of genes leads to genetic disorders in babies. Let's have a look at the genetic disorders in babies list in the following article and understand the vulnerability of the human race to genes and their expressions.
  • Pompe Disease Treatment
    Pompe disease is caused by an inherited deficiency of an enzyme called acid alpha glucosidase. Pompe disease treatment involves a team of doctors and therapists as the disease starts affecting many of the body's systems and organs. Read on to know more about pompe disease symptoms and treatment...
  • Mitochondrial Disease Symptoms
    Mitochondrial diseases are referred to as genetic diseases, as they arise due to damaged mitochondria. Leaf through this article to know more about mitochondrial disease symptoms in infants, children and adults.
  • Mitochondrial Myopathy
    Mitochondrial myopathy is a group of diseases that is being read about more and more with every passing day. If you want to know about it as well, check out this article, that has information on the causes, symptoms and treatment. Continue reading..
  • Autosomal Recessive Inheritance
    What is autosomal recessive inheritance? What are the chances of your family to inherit autosomal recessive genetic diseases? Read this article and find out!
  • Tay-Sachs Disease Symptoms
    Tay-Sachs disease symptoms discussed in the following article, will help you understand the progress of this fatal genetic disorder.
  • Myopathy Treatment
    The nature of myopathy treatment depends on what has caused the condition. The treatment lays its focus on improving the symptoms, and slowing down the disease.
  • Myopathy Symptoms
    Myopathy symptoms primarily include muscle weakness and stiffness. In the following article, we shall learn a bit in detail about the various myopathy symptoms according to the types.
  • Neurofibromatosis Symptoms
    The nature of neurofibromatosis symptoms depends upon the type of the disorder. The disease exists in three different types. So read this article and know about the types and their symptoms.
  • Genetic Disorders in Children
    Genetic disorders in children are not that rare anymore, almost in every block on every street we see a kid with these disorders. Most people generally don't understand the reason behind their unusual appearance and behavior. In this article we learn about common and rare genetic disorders affecting children.
  • Hereditary Diseases List
    The hereditary diseases list is an endless one. However in this article, you can find a few genetic disease examples.
  • Epicanthal Folds
    Epicanthal folds, also known as epicanthus, are a common feature for people with East Asian descent. But, for others it is the result of some other congenital disorders. To know more, read on...
  • Types of Genetic Disorders
    What are the different types of genetic disorders is one question that is asked by many students. If you too are searching for some information related to types of genetic disorders, then the following article will be a useful read.
  • Werewolf Syndrome
    Werewolf syndrome is one of those rare and unusual genetic disorders that cause abnormal hair growth on the body. Read on to know more about the same.
  • Epidermodysplasia Verruciformis
    Epidermodysplasia verruciformis is an extremely rare skin disorder that has a genetic connection. Scroll down to know more about the causes, symptoms and treatment of this skin condition...
  • Common Birth Defects
    Birth defects are those defects that are congenital in nature and that have a high incidence rate. Given below are details regarding common birth defects and their causes...
  • High Ferritin Levels
    What causes a rise in ferritin levels? What are the symptoms of high ferritin levels? How can it be treated? The following article answers all your queries.
  • Birth Defects List
    A birth or congenital defect refers to the deformity a child is born with. Through the following article let us take a look at the facts and examples of birth defects.
  • Albino People
    Albinism is a rare genetic disorder. Find out more about albino people and their life in this article.
  • Angelman Syndrome Symptoms
    Angelman syndrome symptoms comprise slow mental and physical developments. Children born with this disorder walk with jerky movements and are chirpy people, who can be easily conduced to laugh.
  • Brittle Bone Disease Symptoms
    Learn about brittle bone disease symptoms, the life expectancy of a person with brittle bone disease and what exactly causes it. Understand the different categories of this disease and their individual symptoms.
  • 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 that are often noticed in human beings.
  • 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.
  • 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. It 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 Treatment
    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 Treatment
    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.
  • 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.
  • 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 the 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 albinism facts.
  • 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, ongoing researches on treatment for rare genetic diseases and disorders.
  • 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.
  • Genetic Diseases: List of Genetic Disorders
    Genetic diseases, often known as hereditary diseases are caused due to abnormalities in genes. Let us have a look at the few of them in this list of genetic diseases.
  • Trisomy 18 (Edwards Syndrome)
    Trisomy 18 also known as Edwards Syndrome is genetic disorder. This severe condition is caused by the presence of extra copy of chromosome 18 present in the cell attached to original pair.
  • Trisomy 13 Syndrome (Patau Syndrome)
    Trisomy 13 syndrome also knows as Patau Syndrome is a chromosomal abnormality due to the gaining of extra copy of chromosome 13. The median age in this abnormality is only 2.5 days.