Know Your Body Health | Explore More About Genetics Cancer

As we all know that there is one hazardous that has a rapid increase in years of diseases, i.e cancers that affect women. It includes several diseases such as cervical, ovarian, uterine, vaginal, and vulvar cancers. There is no screening test recommended for any genealogical cancer except for cervical cancer. Knowing your own body, recognizing that something may be wrong, and seeing a doctor may be life-saving tasks at that critical time.

  • Why it is important to know about medical history?

It’s also important to know your genealogical medical history. This gives you important clues in finding out if you have an increased chance of developing certain cancers, including ovarian, uterine, breast, and colorectal cancers. Sharing your family genealogy with your doctor can help prevent, detect, and manage these hazardous cancers.

  • Cancer in genes?

Having several close family members with a history of breast cancer etc, ovarian, uterine, or colorectal cancers may suggest that you could benefit from genetic counseling. And ovarian cancer syndrome has an increased risk for breast cancer, ovarian, and several other cancers. People with this syndrome have mutations (changes) in their BRCA1 or BRCA2 DNA. In addition to increasing risk for breast and ovarian cancers, mutations in BRCA1 and BRAC2 also increase the risk for the fallopian tube, peritoneal, and pancreatic cancers in women, as well as prostate cancer in men.

Usually, women with Lynch syndrome are at increased risk for uterine, colorectal, and ovarian cancers. Usually, humans with Lynch syndrome have close relatives who were diagnosed with these cancers, most often before age 50.

If you think you have a raised risk for these cancers, talk to your expert’s doctors and discuss whether DNA counseling is right for you. Once you see a DNA counselor.

In DNA testing by genealogy, your saliva or blood is examined to see if you have genetic changes that place you at a higher risk for cancer than other women.

You can explore more about family history and cancer (particularly gynecologic, breast, and colorectal cancers) by checking out a brand new technique at geneology4u.

Pay attention to your body and know what is normal for you. Gynecologic cancers, attention to your body and know what is normal for you. Gynecologic cancers have when gynecologic cancers are found early, treatment is most effective.

  • Some facts

  • If you have vaginal bleeding that is unusual for you because of when it occurs or how heavy it is, see a doctor right away.

  • If you notice any other unexplained signs or symptoms that last for two weeks or longer, see a doctor.

  • When gynecologic cancers are found early, treatment is most effective.

Why Geneology 4U?

Geneology4u will help you in detecting the diseases in advance that will help you to live a healthy and safe life Please, pay attention to your body and to your family medical history, this September and all through the year. Enroll geneology4u now!

Genome Test For Patients Moves Closer With Genome Analysis Advance by Geneology4u

Diseases caused by DNA changes could be detected more readily thanks to an advance in genome analysis software.

The development will make it easier to integrate DNA testing into health care systems such as the National Health Service of the United Kingdom, which cares for around four million people affected by DNA diseases in the UK.

The website can help you in spoting precise genome changes that cause disease in the more than four billion letters of DNA code that make up the human DNA.

What is the role of the genome test?

It does this by linking to a database of genealogy information from people with genetic diseases to pinpoint genome changes that are known to cause illness.

The software by geneology4u also predicts the consequences of genome changes, helping to identify disease-causing differences that are not already linked to a particular condition.

Also, the software by genealogy scans databases of DNA information from healthy people to rule out DNA differences that look as though they may cause disease but are harmless -minimizing the risk of false diagnosis.

Experts say the geneology4u is particularly useful for diagnosing disorders that may be caused by many different genes, such as severe intellectual disabilities in children.

Using genome to diagnose the diseases in advance is moved to a step closer when advances in DNA sequencing technology made it affordable and possible to decode a person’s genome within a few days.

The sheer volume of data produced—and shortage of expertise—has hampered efforts to analyze it and generate meaningful results.

The new system, which is freely available online, will help to overcome this bottleneck and make it easier to diagnose genetic conditions in clinical practice and research programs.

Why genealogy 4u?

Come and enroll genealogy 4u which has great expertise in the industry of DNA and genome and our future projection is also very impressive through which we can help you to stay healthy and be alert from upcoming diseases in advance.

What is a Genetic Disorder and How it is Defined?

Genetic disease is the disease that is caused by an abnormality in the makeup of the genes of an individual. The genetic abnormality can range from minuscule to major — from a discrete mutation in a single base in the DNA of a single gene to a gross chromosomal problem involving the subtraction or addition of a whole chromosome or set of chromosomes. Some people inherit genetic disorders from the parents, while acquired changes or mutations in a preexisting gene or group of genes cause other genetic disorders. Genetic mutations can occur due to some environmental exposure or can occur randomly as well.

Types of genetic disorders:

  • Single gene inheritance

  • Multi factorial inheritance

  • Chromosome abnormalities

  • Mitochondrial inheritance


  • Single gene genetic inheritance

Single gene inheritance is also known as Mundelein or monogenetic inheritance. The Changes or the mutations that occur in the DNA sequence of a single gene cause this type of inheritance.

  • Multi factorial inheritance

This type of inheritance disorders are caused by a combination of environmental factors and mutations in multiple genes

Examples of multi factorial inheritance diseases are:

  • Diabetes

  • Cancer

  • Obesity

  • High blood pressure,

  • Heart rate

  • Arthritis

  • This inheritance also is associated with heritable traits such as height, eye color, fingerprint patterns, and skin color.


  • Chromosomal abnormalities

In this type of genetic inheritance, distinct structures made up of protein and DNA, are present in the nucleus of each cell. As we know, chromosomes are the carriers of the genetic material, abnormalities in chromosome number or structure can result in disease. This type of abnormalities typically occurs due to a problem with cell division.

  • Mitochondrial genetic inheritance

Mitochondrial genetic inheritance is caused by changes in the non-nuclear DNA of mitochondria. Mitochondria are tiny circles or rod-like organelles that are involved in cellular respiration and found in the cytoplasm of plant and animal cells. Each mitochondrion may contain 6 to 12 circular piece of DNA. This process makes the use of egg cells, but not of the sperm cells, that keep their mitochondria in the process fertilization, this type of DNA is always inherited from the female parent.

Why geneology4u?

Most genetic diseases are the direct result of the change in one gene. But the most difficult problems ahead is to further describe how genes contribute to diseases that have a complex pattern of inheritance, Genealogy 4u will help you to learn about these inherited diseases in advance and helps you in protecting you from that kind of harmful diseases such as in the cases of diabetes, asthma, cancer, and mental illness. In all such diseases, no one gene has the yes/no power to say whether a person will develop the disease or not. Change is required before the disease is diagnosed. to know more about genealogy enroll Geneology4u now!!

The Genetics Diabetes – A Growing Burden in The Society

Metabolic problems arise when abnormal chemical reactions disrupt the systematic breakdown of food into usable forms of nutrients for the body. Such problems result in an imbalance in the hormones required by one to stay healthy. Diabetes, one such metabolic problem, is a chronic disorder that occurs either when the pancreas does not produce enough insulin or when the body is not able to effectively use the insulin it produces. Insulin is a hormone that regulates blood sugar.

Hyperglycemia, or raised blood sugar

It is a common effect of uncontrolled diabetes and over time leads to serious damage to many of the body’s systems, like vascular dysfunction, heart failure, neuronal damage, kidney failure, and blindness.

Globally, 400 million people suffer from this blood sugar disease; this number is estimated to be 692 million by the year 2030. 80% of people with diabetes live in low- and middle-income earning areas. In 2013, diabetes was the direct cause of 1.8 million deaths. In 2015, this number rose to 5.9 million, with 10% of adults, 18 years and older suffering from diabetes. The number of people with type 2 diabetes is increasing in every country and the greatest number of people with diabetes is between 45 and 60 years of age. 200 million people with diabetes are still undiagnosed.

About 6%-8% of diabetes has underlying genetic causes. An example of this kind of diabetes is Maturity Onset Diabetes of the Young (MODY), a monogenic form of diabetes caused by mutations in the dominant gene that disrupt insulin production. They result from interactions of multiple gene variants each exerting only a modest effect, and the environment thus genes are called polygenic.

Genetic testing of diabetes

Genetic testing for sugar or diabetes is now a reality. newborn infants with diabetes in the blood are now being immediately genetically tested for all implicated genes while previously they would only get genetic testing years after diabetes was diagnosed, after which the genes would be tested one at a time. unfortunately, this means that the genetic diagnosis is made early, giving the doctor information about how best to treat the patient and inform them of the medical problems the patients are likely to develop in the coming time.

This is a paradigm shift in how genetic testing fits in with the patients’ symptoms. In the earlier time, symptoms were used to select which gene would be evaluated first – now the early comprehensive gene testing means that the genetic result predicts clinical features that have not yet developed. This helps the doctors to anticipate the existing problems for their patients and put the appropriate health care in place to reduce their effect.

Geneology4u solutions

A provider of clinical genealogy solutions, our genetic testing panel will help you in detecting the genetic disease in an early stage thereby making healthy a lifestyle possible.

Did Your Ancestors Have Cancer? Know Your Family’s Cancer History

Knowing your family health history is important especially when you have been diagnosed with a cancer

What is genetic cancer?

Genetic cancer means that a person was born with a hereditary mutation, or change, that makes this person more likely than usual to get that genetic cancer. This hereditary mutation could have come from either the paternal or maternal side both. Genetic cancer may also be called hereditary cancer or cancer in the family.

Around 8% to 24% of all cancers are due to genetics. This is a very small percentage of cancers, so how can you tell whether cancer is in genetics?

We have some rules to identify cancer:

Having several relatives with cancer on the same community of the family, especially if they were diagnosed at a younger age

Having a single member in the family with multiple tumors, especially in the same body part.

Hereditary testing for genetic cancer

Genetic cancer is found through hereditary testing. This is the test of a person’s genes, proteins, or chromosomes. Analysis can:

  • Help in predicting the risk that someone will get a genetic disease.

  • In detecting carriers of the disease. These are ones who do not have the disease but have a copy of the disease gene.

  • Diagnose a genetic disease.

  • Find out the likely course of a disease.

Hereditary testing is done by taking a sample of tissue or blood that contains genetic stuff, such as the cells inside a person’s cheek. More than 1000 hereditary tests are available for many different diseases, including the brain, ovarian, colon, thyroid, breast, and other cancers. Learn more about hereditary testing.

What your genetic research of cancer can show

Information from your family’s research can help a doctor to determine whether:

  • You or others in your family may benefit from hereditary counselling. This is functional counselling that explains the risks of transferred cancer and the causes, risks, and limitations of genetic testing.

  • You or others in your family may benefit from hereditary testing.

  • You need more demanding care than people with non-genetic cancer, even if you do not need hereditary testing.

This is how you can protect yourself by detecting genetic cancer in advance and you can prevent yourself by discussing your family health history with your health care doctor. This is especially true if you have been diagnosed with cancer. To know more about family lineage visit Geneology4u.