genetic disorder

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genetic disorder

n.
A pathological condition caused by an absent or defective gene or by a chromosomal aberration. Also called hereditary disease.

genetic disorder

ge·net·ic dis·or·der

(jĕ-net'ik dis-ōr'dĕr)
A widely used but nonetheless imprecise term that denotes a condition or illness related to biologic inheritance.

Patient discussion about genetic disorder

Q. what makes Arthritis a genetic disease?

A. First of all, the term arthritis is a bit inaccurate: Arthritis denotes an inflammation of joints. There are many kinds of arthritis that may result from different causes, and therefore, are different diseases: septic arthritis (inflammation due to infection of joint) has much less genetic background than ankylosing spondylitis (an arthritis of the lower back joints that occurs almost exclusively in people with certain genetic background).

The arthritis with the genetic background are usually the autoimmune ones: Due to genetic determinants, the immune system of some people is programmed to recognize the various parts of the joints (and other organs as well) as foreign (i.e. like bacteria) and thus launches an attack on them. In normal immune system, that doesn't happen.

You may read more here:
http://en.wikipedia.org/wiki/Autoimmune_disease

Q. Is bipolar disease a hereditary problem? My only son is in his teens that is the age to enjoy life, but he cannot enjoy his life with his friends because we found that he is suffering from a bipolar condition. I feel so sad for him and though my care-free days have gone, I often think about how much fun I had at his age. I too suffered from a bipolar disorder and my mom too. Is bipolar disease a hereditary problem? I want him to help to enjoy his life.

A. I agree with you. No one should suffer because of hereditary problems. This is the same situation here as genes are passed from generation to generation. This information is inconclusive because many who may have had bipolar disorders did not have it checked out. Who is to say, how many people 50 years ago had it but dismissed it as being moody, or ill tempered. Doctors were not aware about this problem years ago. Some time back, someone who showed signs of a mental disorder was straight away shoved into a mental hospital and left to suffer. Besides they are often treated with electric shock therapy eventually getting out of control. Testing is still in progress to find out if genetics play a role but these theories may take several more years before they can have a better understanding.
http://www.youtube.com/watch?v=f7uKg7ujoig&eurl=http://www.imedix.com/health_community/vf7uKg7ujoig_film_mental_illness_released_strive_happiness?q=bipolar%20disease%&feature=player_embedded

Q. Is FMS heredetery? My mother was diagnosed with FMS and I would like to know what are the chances I’ll have it too.

A. Hereditary is not the right term. It’s not a genetic disease but The cause of fibromyalgia remains elusive. However, recent studies show that genetic factors can predispose individuals to a genetic susceptibility to fibromyalgia.

More discussions about genetic disorder
References in periodicals archive ?
com) Rhythm is a biopharmaceutical company focused on developing peptide therapeutics for the treatment of rare genetic deficiencies that result in lifeCaethreatening metabolic disorders.
In addition to the genetic deficiencies, there are nutritional deficiencies [in B vitamins]," Dr.
In addition, a small number of hemophilia patients have also been described as having co-inherited genetic deficiencies in protein C itself.
Earlier studies had linked genetic deficiencies in MAOA production to extreme aggression in mice and in men of a Dutch family.
Cell Genesys is currently evaluating liver-directed AAV gene therapy in animal studies of both types of hemophilia -- hemophilia A and B -- which result from genetic deficiencies in blood clotting factors VIII and IX, respectively.
All states require that newborns be screened for a limited number of genetic deficiencies before being discharged from the hospital.
Setmelanotide is a potent, first-in-class MC4 agonist in development for the treatment of obesity caused by genetic deficiencies in the MC4 pathway, a key pathway in humans that regulates energy expenditure, homeostasis, and appetite.
Their hope is eventually to implant engineered cells into humans as a means of correcting certain genetic deficiencies.
The correction of genetic deficiencies in stem cells may have utility in a number of other genetic diseases.
which is developing setmelanotide (RM-493), a novel peptide MC4 agonist for the treatment of obesity caused by genetic deficiencies in the MC4 pathway.
The research suggests that physicians may someday treat genetic deficiencies of certain circulating proteins by implanting "colonies' of specially engineered protein-secreting cells.
These genetic deficiencies, or inborn errors in metabolism, are orphan diseases that have severe consequences for patients.