Genetic Explanation of Depression Research on the heredity of depression within families shows that some individuals are more likely than others to develop the disorder. If you have a parent or sibling with depression, you may be 1.5 to 3 times more likely to develop the condition than those who do not. This suggests there may be some kind of genetic influence. Gershon 1990 studied 10 families, and found rates of MDD in first degree relative ranged between 7-20%, which i considerably higher than the rest of the population. Weisman 1984 also found that relatives of people diagnosed with depression before the age of 20 had 8x greater chance of being diagnosed with it.
The main symptoms include: muscle spasms, urinary problems, mood and behavior issues, and fatigue. Each episode can last for days, weeks, or months. Episodes alternate with times of reduced or no symptoms. Fevers, hot baths, sun exposure, and stress can trigger or worsen attacks. Patients with multiple sclerosis can have symptoms in several parts of the body, because nerves in any part of the brain or spinal cord may be damaged.
Citizens from the ages of 14 to 49. Here is a small break down of how HSV-2 affects different ethnic groups, men and women. “HSV-2 infection is more common among women than among men (20.9% versus 11.5% in 14 to 49 year olds). Infection is more easily transmitted from men to women than from women to men. HSV-2 infection is more common among non-Hispanic blacks (39.2%) than among non-Hispanic whites (12.3%) or Mexican Americans (10.1%).
Other symptoms can include anemia, chronic fatigue or pain syndromes, migraines, nerve problems, infertility or miscarriages, and other apparently unrelated conditions. Patients are frequently misdiagnosed as having Irritable Bowel Syndrome (IBS), spastic colon/bowel, or Crohn's disease." Here are a few more symptoms associated with Celiac Disease as stated in a CNN broadcast by Heidi Collins on 15Oct 2007. Malnutrition, infertility, Cancer, thyroid disease, Osteoporosis, Pregnancy complications, and Depression If you have any of these symptoms you might be interested in knowing about the testing
Symptoms of NF2 may include hearing loss, ringing in the ears, dizziness, balance problems, headaches or seizures. Early removal of small auditory nerve
There are also 7 conditions which have symptoms that are similar to MS making it even harder to be able to diagnose it. Also if you have only suffered one attack of symptoms associated with MS, then it is hard to try and diagnose it. But once someone has had a relapse of the symptoms then they are able to diagnose it for sure. Ways to diagnose it: Neurological examination: your neurologist is there to look for changes or any weaknesses in your eyes, leg and hand co-ordination, balance, speech and your reflexes. This will show if your nerves are damaged.
MD causes the muscles to become weak or even die. The majority of the different forms of MD can also affect the heart, gastrointestinal, nervous system, endocrine glands, as well as the eyes and brain. It was in the 1860’s when this disorder became prominent in the medical field. The most common, yet most severe form (Duchenne muscular dystrophy), was studied by a French neurologist by the name of Guillaume Duchenne. There are a variety of different types of muscular dystrophy that can occur as a child or as an adult that include: Becker muscular dystrophy, Duchenne muscular dystrophy, Emery-Dreifuss muscular dystrophy, Facioscapulohumeral muscular dystrophy, Limb-Girdle muscular dystrophy, congenital muscular dystrophy, Oculopharyngeal muscular dystrophy, distal muscular dystrophy, and Mytonic dystrophy.
Only 40% of patients with CRPS have serum antineuronal antibodies, and inflammatory cytokines might be most relevant if pinprick hyperplasia is present. Future studies should focus on patients who have these characteristics to form a more accurate conclusion. Only 3 out of 13 patients had a very positive response, the remaining 10 patients has no or only minimal response. They believe if they were able to identify patients likely to respond, the efficiency of treatment and the cost-effectiveness ratio might be greatly improved. Only then might IVIG offer what they have long been looking for: a safe, effective, easy to adhere to, and scientifically validated form of treatment for
GAD tends to appear gradually. The first symptoms most likely happen between the childhood and middle age years. Physical signs/symptoms of GAD are: Lightheadedness, racing or pounding heartbeat, tiredness, revisiting headaches, aches of the muscles, hard time swallowing, body trembles, shakiness, hot and cold sweats, nausea and frequent urination. Mental signs/symptoms of GAD are: anxiety, trouble concentrating, irritability, startled easily, awareness of inappropriate anxiety, and some cases depression. Both physical and mental symptoms/signs of Generalized Anxiety Disorder can change, depending on how your body reacts at a certain time.
They could range from mild, moderate to severe. Some of these symptoms include fatigue, incoordination, spasticity, sensory loss and numbness, muscle weakness, cardiovascular dysautonomi, heat sensitivity, blurred vision, tremor, impaired sudomotor function, bladder dysfunction, cognitive or memory deficits and possible depression (Castellano, V. 2006). Most of the disability that is affiliated with multiple sclerosis is caused by the nerve fibers in the long pathways, like the pyramidal tract. This tract supplies the efferent and afferent signals to the legs and dorsal columns. With damage, it is not able to successfully send the signals, causing motor disability (Gutierrez, G. M. 2005).