Events Calendar

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12:00 AM - Hepatology 2021
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World Nanotechnology Congress 2021
2021-03-29    
All Day
Nano Technology Congress 2021 provides you with a unique opportunity to meet up with peers from both academic circle and industries level belonging to Recent [...]
Nanomedicine and Nanomaterials 2021
2021-03-29    
All Day
NanoMed 2021 conference provides the best platform of networking and connectivity with scientist, YRF (Young Research Forum) & delegates who are active in the field [...]
Smart Materials and Nanotechnology
2021-03-29 - 2021-03-30    
All Day
Smart Material 2021 clears a stage to globalize the examination by introducing an exchange amongst ventures and scholarly associations and information exchange from research to [...]
Hepatology 2021
2021-03-30 - 2021-03-31    
All Day
Hepatology 2021 provides a great platform by gathering eminent professors, Researchers, Students and delegates to exchange new ideas. The conference will cover a wide range [...]
Annual Congress on  Dental Medicine and Orthodontics
2021-04-05 - 2021-04-06    
All Day
Dentistry Medicine 2021 is a perfect opportunity intended for International well-being Dental and Oral experts too. The conference welcomes members from every driving university, clinical [...]
World Climate Congress & Expo 2021
2021-04-06 - 2021-04-07    
All Day
Climatology is the study of the atmosphere and weather patterns over time. This field of science focuses on recording and analyzing weather patterns throughout the [...]
European Food Chemistry and Drug Safety Congress
2021-04-12 - 2021-04-13    
All Day
We invite you to meet us at the Food Chemistry Congress 2021, where we will ensure that you’ll have a worthwhile experience with scholars of [...]
Proteomics, Genomics & Bioinformatics
2021-04-12 - 2021-04-13    
All Day
Proteomics 2021 is one of the front platforms for disseminating latest research results and techniques in Proteomics Research, Mass spectrometry, Bioinformatics, Computational Biology, Biochemistry and [...]
Plant Science & Physiology
2021-04-17 - 2021-04-18    
All Day
The PLANT PHYSIOLOGY 2021 theme has broad interests, which address many aspects of Plant Biology, Plant Science, Plant Physiology, Plant Biotechnology, and Plant Pathology. Research [...]
Pollution Control & Sustainable 2021
2021-04-26 - 2021-04-27    
All Day
Pollution Control 2021 conference is organizing with the theme of “Accelerating Innovations for Environmental Sustainability” Conference Series llc LTD organizes environmental conferences series 1000+ Global [...]
Events on 2021-03-30
Hepatology 2021
30 Mar 21
Events on 2021-04-06
Events on 2021-04-17
Events on 2021-04-26
Articles

Are Your Medical Conditions Hereditary?

Exclusive article by Lindsey Patterson at EMRIndustry

 

When you are suffering from a disease, it is natural to wonder if you inherited it and if the disease can be passed down to your children. Most diseases and disorders are spread by person-to-person contact and poor immunity systems. There are still a lot of diseases that are genetic. These stem from abnormalities in your genetic makeup. It can range from a small mutation from a single gene to a severe deformation of entire chromosomes. Environmental exposure can cause genetic mutation that can be passed to your children.

Heredity is built by your genes. You get your genetic makeup from your parents, and you will pass yours to your children. Genes contain DNA which is the framework for protein production in the body. Your body needs protein to do the necessary work in its cells. Protein acts like the maintenance department for your cells.

If there is a mutation in the cells, your genes can be affected. It can confuse the DNA instructions for protein. Sometimes, too much protein can be produced or none at all. This genetic mix-up creates a medical condition known as a genetic disorder. It is possible for you to get a gene mutation from your father, your mother, or both. You may also experience a mutation during your adult years that can affect the children you conceive. Here are the different types of genetic disorders:

Single Gene Mutation

This inheritance is also referred to as monogenetic or Mendelian inheritance. In these cases, only a single gene is mutated within your sequence of DNA. Scientists have labeled at least 6,000 of these monogenetic disorders. Out of every 200 births, at least one baby can be affected by a single gene mutation. The most familiar monogenetic diseases include sickle cell anemia, Marfan syndrome, cystic fibrosis, hemochromatosis, and Huntington’s disease. The mutated gene may be recessive, dominant, or X-linked. Although there are treatments that deal with some of the symptoms of monogenetic diseases, there are no cures.

Complex Inheritance

In some people’s genetic makeup, a number of genes can be affected. This can be caused by factors in the environment or multiple mutations. You may be suffering from one of these common complex inherited disorders: various types of cancer, arthritis, coronary disease, hypertension, diabetes, or Alzheimer’s disease. Obesity, which can be a factor in all of these disorders, is also a complex inherited disease. Some disorders, like shingles, are more likely to affect people who have close relatives with the disease, claims a report by MedicalNewsToday.com. Shingles treatment can ease the symptoms.

Mutated Chromosomes

In the nucleus of every cell in your body, a mixture of protein and DNA make chromosomes. According to the National Library of Medicine, humans have 23 pairs of chromosomes. They are responsible for carrying your genetic material. If you have an abnormality in the number of your chromosomes, you can get a disease. It is caused by the cells in your body not dividing properly.

A good example of an inherited disease from mutated chromosomes is Down’s syndrome. This disease affects the 21st chromosome and multiplies it by three. Other types of these diseases include Cri Du Chat syndrome, Turner syndrome, and Klinefelter syndrome. Sometimes, parts of two chromosomes are exchanged and cause an inherited disease.

Mitochondrial inheritance

There are some inherited diseases that are caused by mitochondria mutations. The non-nuclear part of the mitochondria are affected. They are minute, rounded organisms that are responsible for cellular respiration. Mitochondria are contained in the cytoplasm of human, animal, and plant cells. There can be between 5 to 10 DNA pieces in each mitochondria. These types of inherited diseases are always passed down through the mother, since sperm cells do not keep their mitochondria during fertilization. Some examples of these disorders include optic atrophy (Leber’s disease), MELAS dementia, and myoclonic epilepsy.

If you have a parent or another close relative with a certain condition, you can speak with your doctor about it. The doctor can run tests to see if you have the disease or are prone to pass it on to your children. Some inherited disorders can be cured if caught in the early stages.