Doctor insights on:
Disease Of Aids
Yes: Co infection with hepatitis b or hepatitis c ( that is having HIV and either of the above) is documented to generally result in further progression of both diseases. Therefore, patients with either illnesses must be screened to rule out co infection... Treatment is encouraged for both viral illnesses. New treatments are available for hepatitis c. ...Read more
Different stages: You can have the rash called erythema chronicum migrans after the tick bite. This is the intiial acute infection and characteristic rash If it is not detected then it can incubate in your body and cause later sequela such as arthritis adn other systems can be invovled. There are blood tests that can be done to help clarify the diagnosis. Your physician can test for Borrelia Burgdoreri. ...Read more
There's a New One: Besides the expected mild, moderate, & severe very nicely described by dr. Nash, there is now officially a 4th category --- mild cognitive impairment (mci). This is a stage before mild & the thinking is that here would lie your best bet at preventative strategies (if & when we find some of those). ...Read moreSee 2 more doctor answers
YES !!: Huntington's disease (named after the long island doctor who described it ) has dementia , chorea (a dance like involuntary movement) and family history as its main features it is transmitted by a dominant gene (50% chance of it occuring in the offspring). It is at present incurable although the movements can be modified by medication. ...Read more
Flu-like symptoms of: sore throat, fever, nausea & vomiting in some, but infection with any serotype of poliovirus may not cause any symptoms in an immune-competent person. If the virus causes meningitis, add headache, stiff/sore neck & back, lethargy & risk of paralysis of the legs & other muscles including the diaphragm. I've seen kids die of poliomyelitis & other vaccine-preventable illnesses. I may see it again. ...Read more
Really variable: Please let us know the particular disease so that we can provide you with that information. Can re-ask. ...Read more
A prion disease: Cjd is caused by infection/exposure to an abnormal form of the prion protein (pp). The abnormal form of pp is a completely bent out of shape version of the normal pp . This abnormal shape is very hard for the protein to change to spontaneously, but this can happen (1 in a million people). Once changed the abnormal pp changes other pp's and so on as the disease rapidly spreads/kills the brain. ...Read moreSee 2 more doctor answers
What are the signs and symptoms of pathogenic diseases, hereditary diseases, deficiency diseases and physiological diseases?
Site protocol: You get the most from this site when you provide background information on a medical problem and ask a related but clear question. We are not a shortcut for homework assignments, or a library reference section. For that you need to consult your local library or text books. ...Read moreSee 1 more doctor answer
See below: There is only one mutated copy of the gene needed for a person to be affected. Each affected person usually has one affected parent. There is a 50% chance that a child will inherit the mutated gene. It is commonly seen in western european descent than asian or africian ones. ...Read more
Several forms exists: Infantile form: child appear normal until the age of 3-6 mo, when their development slows & muscles used for movement weaken. Affected infants lose motor skills such as turning over, sitting, and crawling. They also develop an exaggerated startle reaction to loud noises. As the disease progresses, seizures, vision&hearing loss, intellectual disabilities¶lysis may appear with abnormal eye exam. ...Read more
Tremor: Early, there may be a resting tremor unilaterally, and perhaps some focal stiffness. Later, the gait may become impaired, with short unsteady steps, and a tendency to fall. The face may become expressionless, drooling may present, and thinking becomes disrupted. Problems with swallowing, constipation, and skin eruptions can also occur. ...Read more
How are causes and onsets of symptoms of huntington's disease different from those of pku and tay sacks disease?
Too broad a question: There are all inherited disorders with the common issue of neurologic impairment, hd in adults, pku and ts in children. The neurologic damage in pku can be prevented with diet, but there is no treatment for hd and ts. Tests are available to detect carrier status in all of these. ...Read more