Burning mouth syndrome, occurs in the oral mucosa is a burning kind of pain without obvious clinical signs of the syndrome-positive. The etiology is unclear, may be related to emotional and mental state.
Cause
Lead to the cause of burning mouth syndrome is more complex, experts say the following three main factors, psychological factors which prominently.
First, the local factors
Such as residual root and crown, poor restorations, denture materials, Allergies, stones, excessive drinking, smoking and other physical and chemical stimuli. Frequently Shenshe self myofascial tension or strain caused by the tongue caused by local pain.
Second, the system factors
The most common is the menopause syndrome, followed by Diabetes, vitamin and mineral deficiencies, long-term abuse of flora caused by antibiotics, leading to Candida albicans infection, long-term use of anti-anxiety drugs, diuretics, etc.
Third, psychological factors
And the person's character, such as multi-anxiety type, depressive, emotional instability, but not with the psychological fear of cancer, a survey, more than 75% of tongue cancer pain patients worry, 37% of patients occasionally found in the tongue edge of the the roots of "small disputes" in the back of the leaf-nipple and tongue papillae, worried that she is suffering from a terrible disease, frequent self in the mirror, into a "self-test - panic - and then self - even panic - - tongue pain increased, "the vicious cycle. Therefore, we in the treatment of tongue pain patients, except for cause, symptomatic treatment, the more important point is that psychological treatment and suggested treatment, because this effect is to improve and consolidate the key.
Diagnosis
1. Burning kind of pain can occur in any part of the oral mucosa, and many have no fixed boundaries.
2. Pain severity and emotional and mental state, and increase the features of the morning light the afternoon, the pain can be a natural ease.
3. Local examination without congestion erosion, ulcers and other diseases.
4. May be associated with irritability, depression symptoms.
Principles of treatment
1. Mental sulfur guide treatment.
2. With the obvious irritability, sedation can be used in patients with depressive symptoms with antipsychotic drugs and drugs such as oryzanol regulate autonomic function.
Because vaccines have been produced and administered, and now the disease is slowly being eradicated - in countries that can afford to vaccine people for free.
Thrombotic thrombocytopenic purpura (TTP) is a rare blood disorder characterized by excessive clotting throughout the body's small blood vessels. This clotting can lead to a decrease in platelet count, causing anemia and symptoms like bruising, bleeding, and organ damage. TTP is considered a medical emergency and requires prompt treatment to prevent complications.
For female it probably will be 82, but if that women has medical conditions its rare that the women would live up to 80. For male it would be about 75, if that man has medical conditions it would be more severe than a women's medical condition. About 70.
It is very rare for someone to defecate in their sleep unless they suffer from a medical condition that affects bowel control, such as a form of incontinence. However, there have been cases where people have experienced involuntary bowel movements during sleep, though it is not typical.
Hi,all I can add to this question is that I feel it is quite possible that pots and shy-dragers multiple system atrophy,primary autonomic failure could all just be the same things. I was diagnosed with Primary autonomic Failure(possible Pots) just recently and am treated with fludro-cortisone,beta blockers and salt etc Also the waist high surgical stockings. My Neurologist says they can only watch for a long period of time and treat symptoms. It is extrenely rare and they are watching me for shy-dragers. That, from what I can understand from my G.P. is what happens with these disorders. Takes time to reach a full diagnosis of Shy-dragers or M.S.A. and most of the time it is diagnosed after an autopsy. I hope this helps but if you could add anything to help my understanding,as I am new at this,diagnosis.(Not the debilitating symptoms), I would appreciate any input. My Neurologist told me that I must know my own disease as there won't be many (in the medical profession) who will know it. So, from that I have had to do a lot of research etc. As well as know my body well., and know my limitations etc.
It is a disease of the arteries of the brain.... That requires surgery..... It is extremely rare.....
I have it, it is actually not hereditary it is a birth defect. Extremely rare and completely random.
In the United States, the most common age for Reye syndrome is six to eight years. Reye syndrome is extremely rare in individuals over the age of 18.
Stiff person syndrome (SPS) is an extremely rare progressive neurological disorder characterized by persistent rigidity and spasms of certain voluntary muscles, especially those of legs and feet.
Juliana Wetmore is a little girl who suffers from Treacher Collins Syndrome which is an extremely rare genetic syndrome. There have been no updates on her since about 2012 and they were discussing that they were finally going to give her cheekbones.
no it is an extremely rare type of lymphoma
it can be, but it is rare.
middle child syndrome is very rare. But you have got it.
Black Coral is rare, extremely rare...
extremely rare
Toucans are not extremely rare or endangered.
YES! They are EXTREMELY rare!