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GENETIC CONDITIONS  

In a world where the cost of healthcare is skyrocketing, should an insurance be able to access your genetic records and deny coverage based upon these genetic records?

For children who suffer from genetic predisposition for cutaneous melanoma, there is a need to begin aggressive screening as early as 10 years of age.

Intersex people are often grouped with the gay, lesbian, bisexual and transgendered community, although somewhat unfairly.

A new study has proven that 1% of autism cases are genetic and some media outlets are using that to vindicate environmental causes such as vaccines raising more questions than giving answers to in the autism community.

Ellis van-Creveld Syndrome is an inherited genetic form of dwarfism often characterized by extra fingers or toes. Intelligence is usually not affected, and these children are capable of living a happy, rewarding life.

According to researchers from Leiden University Medical Centre in the Netherlands, patients who suffer from an extremely severe form of migraine, one in which one side of the body becomes very weak, might benefit from undergoing genetic testing.

Sulforaphane, a natural compound found in broccoli could be an important source of treatment for the genetic skin disorder called epidermolysis bullosa simplex (EBS).

Offering an overview of the genetic defect known as Machado-Joseph disease and the impact on the CNS beginning in childhood or adolescence.

Do You Think Genetic Altering is Right or Wrong?

Nutrigenetics is the study of how our genetic makeup influences our responses to diet. Several companies attempt to commercialize the results of nutrigenetic research.

Rett's Syndrome is a genetic disorder that occurs on the X chromosome that most often occurs in females.

A genetic reason for not vaccinating is a look at how nature has preserved the species of life including humans. We are trying to circumvent one of the most crucial building blocks of life, the immune system but in the end it could be catastrophic.

Many people think obesity is caused by genetic factors. But is this true? Or are genetics just one factor among many?

For children who are diagnosed with the genetic disorder, 22q11 Deletion syndrome, it is important to manage health care early in life.

A new genetic marker for Autism Spectrum Disorder is one more step on the road to understanding this condition.

RLS is a poorly understood illness. Until now it is believed to be a neurological issue. Two studies confirm its genetic basis.

Because of advances in knowledge of genetic components of illness, new technology has been invented that gives doctors ability to measure C-reactive protein. This has predictive value for vascular disease, and therefore probable leads to prevention.

As a rare genetic disorder, victims of Batten disease suffer a shorten life span. This is an overview of the childhood disorder.

Information about what is involved in genetic counseling and why an individual might consider consulting a specialist.

Often affecting the Jewish population of Eastern European decent, Gaucher Disease can lead to life long health complications

As a genetic disorder, some children may experience amelia in result to trauma or infection but most experience the complication in response to a genetic complication.

Scientists announced a genetic breakthrough in pinpointing those at higher risk for developing Restless Leg Syndrome (RLS) and Periodic Limb Movements (PLM).

Proper eye care is important for canines and some dog breeds are predisposed to genetic eye diseases. Symptoms and treatment of common eye conditions in dogs.

People who suffer from ACHOO syndrome commonly will sneeze excessively, approximately 30 to 40 times, when they look into a bright light.

This paper will inform readers of the benefits studying behavioral genetics has for thousands of people with behavioral disorders. People with autism and dyslexia will be focused on specifically.

For children born with neurofibromatosis, early diagnosis and treatment is important to overall health.

A gene mutation is the cause of Alstrom syndrome. This gene that is affected is the ALMS gene.

Parents who have an autistic child will be encouraged when they hear that researchers are working on new treatents for these children.

The first study that tackles a genome-wide study for HIV treatments and vaccines was published recently in the journal Science Express.

Ever notice that medical miracles only apply to cancer, emerging from comas, and recovery from heart attacks? What about all those other diseases that are always 100 percent fatal?

A trained esthetician can help guide a client to proper skin care. Knowing a client's skin type and condition can make the difference between good and great results.

A wondrous scientific achievement? Or an abomination?

Klinefelter's Syndrome is a genetic condition that affects boys and is characterized by the presence of one or more extra X chromosomes. The Internet is a good source of information for finding out more about Klinefelter's Syndrome.

Newborn screenings are vitally important to the growth and development of your child. With this thought in mind, many states have implemented standardized screening processes.

This is an article of the struggles of growing up with the diagnosis and treatment of diabetes and being the parent of a child with a medical condition

This article explains the difference between a congenital defect or abnormality and a hereditary disease or condition.

Quiet, affectionate, and docile, the Hungarian Greyhound possesses a dignified quality and stable temperament.

Determined, resourceful, and mild mannered, the Italian is a quiet breed which does well in calm households.

Marfan syndrome is a disease of the connective tissues that affects many sytems of the body including the cardiovasculat system and thus can be fatal. With rew advances in the medical field sufferers can enjoy a long life for which timely and proper diagnosis is necessary.

A personal look at some of the differences in Late Onset Congenital Adrenal Hyperplasia and Polycystic Ovarian Disease.

Two Very Good Hospitals for Pre-Conception Counseling Services in Akron, Ohio

Overview: The fatal Tay-Sachs disease in babies

Your kidneys are small bean-shaped organs located on either side of your abdomen. They have a wide variety of functions in the body, the most important of which is the regulation of blood pressure.

What if you just found out that your child has mental retardation or another learning disability? What strategies do you use to help them? After living with a cousin who has mental retardation, I learned the stepping stones that can be used to help them and yourself.

Epilepsy is a seizure disorder that can be controlled by anticonvulsants. But, when the patient is unresponsive or can not tolerate drug treatments there is still hope. A recent study shows that a high-fat diet is a promising treatment alternative.

Also known as the Little Lion Dog, the Lowchen has a life expectancy of 12-14 years.

This paper attempts to define the field of bioethics - the ethics that drives all medical desicions. It also gives an overview of the major players in its development: Van Rensselar Potter, Joseph Fletcher, Paul Ramsey, Richard McCormick and Peter Singer

Diabetes mellitus is a group of diseases characterized by high levels of blood glucose. Individuals can take steps to control diabetes and lower the risk of complications such as heart disease, blindness, kidney failure.

Discusses taking a skeptical approach to life, and the benefit and (need) for the justification of beliefs to proportion to empirical evidence as our only defense against a complicated world of varying interests and agendas.

Overgrowth Syndrome is a blanket term covering numerous genetic birth defects, some of which are fatal, many of which lead to cancer.

Scoliosis In The Adolescent

Scoliosis can be defined as a lateral deviation in the spinal column. It occurs in over twice as many females than males and it tends to run in families. It can have many causes.

The Canine Heritage Breed Test can analyze your mixed breed dog's DNA to tell you what breeds are in the mix. Besides satisfying your curiosity, knowing your dog's heritage can help avoid potential health problems.

No longer is autism a condition to be denied by embarrassed parents. Today, we know more than ever before about this developmental disorder. If your child or grandchild is dealing with autism, here's what you HAVE to know about natural and herbal remedies for autism.

The first draft of the horse genome sequence has been deposited in public databases and is freely available to researchers.

For individuals who are at-risk for genetic conditions such as Alport syndrome, the decision to confirm the condition by biopsy is often a difficult one to make.

Genetic test can determine if you'll lose your hair by the age of forty.

Many medical problems plague our population and it's widely discussed and openly presented through many avenues. But, what about the common conditions such as psychiatric disorders? Read this article for an in-depth look...

Common ways to treat and prevent various skin conditions, including eczema and atopic dermatitis.

Victims of a rare genetic disease, epidermolysis bullosa simplex (EBS) had little hope of leading a near normal life. If research done at Johns Hopkins turns out the way they think it will, suffers of this usually fatal disease may have reason to hope.

Mass marketing of genetic sequencing services could change life and medicine. But will it also endanger personal health data, security, and societal and cultural norms? And what will happen to insurance?

The evidence showed that the role of the antioxidants may be to stop a tumor's ability to grow under conditions where they are deprived of oxygen.

Learn the facts on maintaining good health, grooming needs, living conditions and more when it comes to the German Shepherd

There may be a genetic reason for your child's medical problems - why it's important to know and how you can find out.

Current status of the ability to diagnose and treat conditions associated with ambiguous genitalia in neonates.

Dogs have become a growth industry in the keystone state, with a number of dogs brought from breeders showing signs of bad behavior and genetic problems.

A study in the U.K. has identified many genetic markers, some previously unknown, for common diseases.

Certain medical conditions can be troublesome enough to affect daily life. An abdominal migraine is one such condition. They are characterized by sudden attacks of pain around your abdomen. This article will share with you

Millions of Americans are taking prescription medications for mental health conditions. Is all this medication the only way?

Learn the facts on maintaining good health, grooming needs, living conditions and more when it comes to the Cornish Rex Cat

Nail Patella syndrome is a condition which is rare and genetic. This disease affects the nails, kneecaps, and even causes the destruction of the kidneys.

About 13% of all women suffer from infertility. The most common cause is with the most common cause being ovaries that do not function the way they are supposed to and genetic links are suspected in most of the cases.

The herb, eyebright is helpful for many conditions and ailments, most especially those of the eyes.

For many people, it's just easier to blame others. When it comes to genetic traits, and your behaviors, can it all really be traced to the genes that you inherited from your parents, that certain structure of genetic code that made you who you are? Yes and no.

Researchers at the National Institute for Mental Health have evidence that proves that a genetic link exists between schizophrenia and cancer.

Common Variable Immunodeficiency (CVI) is a group of rare genetic immunodeficiency disorders. There are abnormalities in the immune cell development that result in a decreased ability to produce antibodies in response to the invasion of foreign substances.

Turner syndrome is a a genetic disorder that affects only females and prevents them from producing estrogen and other growth hormones. When caught in infancy, TS can be managed and treated with regular medical care.

Autoimmune Lymphoproliferative Syndrome is a rare disease characterized by 3 main conditions.

Many people are unfortunate enough to have to live with debilitating diseases and conditions, that doctors have not yet discovered a cure for.

There should be a form of control or option to help get family history information to the children of adoption

A new study shows that plants have unique, non-genetic environmental adapting mechanisms that are transmitted as cues from the maternal plant.

Newborn screening in Vermont is a program initiated by the Vermont Department of Health that's purpose is to test newborns for disorders that can be the cause of many medical conditions ranging from severe infections to death if not treated.

Fibrous Dyplasia is a genetic disorder that occurs unexpectedly and as a result causes parts of the body to not to function, as they should.

When a child has "charge syndrome", they have a genetic condition that is a result of a mutated gene. This gene that is mutated is the CHD7 gene most often.

Research from Uppsala University shows that if a woman is overweight at the time she becomes pregnant, she will have a greater risk to have a child with ADHD or similar conditions by the time the child is ready to start school.

As a genetic disorder affecting the connective tissues, individuals with Nail-patella syndrome often realize they have the condition with the initial appearance of unhealthy fingernails and toenails.

With many dementia symptoms, it is important to narrow the focus of genetic based dementia symptoms so as to classify them correctly and then apply appropriate treatment.

The researchers hope that one day their discovery might lead to the creation of gene therapies that would reverse or lessen the effects of the largest group of genetic disease in humans called mitochondrial diseases.

With families decreasing in size, many couples seek to select the gender of their children in an effort to ensure the avoidance of hereditary medical conditions, balance of gender within the family unit and even for cultural reasons.

Hemochromatosis is primarily genetic hereditary blood disorder, causes the body to absorb & store too much iron. Excessive amount of iron damage organs, especially the liver. Diagnose by taking blood tests & treatment called phlebotomy.

One in seven adults and thousands of children are aversely affected by arthritic conditions. But there is help, and hope, in nature.

Read further about the rare birth defect that most parents initially believe to be "lazy eye," but that in fact is a genetic abnormality which occurs in the earliest stages of embryotic development.

DNA carries the genetic information necessary for the organization and functioning of most living cells and control the inheritance of characteristics. It is the biochemical molecule that makes chromosomes and genes.

Thalassemia is an overarching term referring to several forms of hereditary blood disorders. The internet is a good source of information for finding out more about this genetic condition:

Cystic fibrosis is a potentially life-threatening lung disease, it affects about 15 babies born in Oregon each year. Oregon is the seventeenth state to make it a requirements that all infants born be tested for the genetic disorder, cystic fibrosis.

This is an overview of the genetic disorder that results in excessive cartilage and cancer in adults after age 30.

The interrelationship between health, safety, and nutrition regarding children is very important. Understanding certain guidelines, and potential hazardous conditions can help prevent physical and emoti