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	<title>Private Doctor Online &#187; Rare Diseases</title>
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	<description>Talk with Your Doctor about Medical health treatment Problems</description>
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		<title>Complete Information on Autoimmune Inner Ear Disease With Treatment and Prevention</title>
		<link>http://www.yourdoctorinfo.com/complete-information-on-autoimmune-inner-ear-disease-with-treatment-and-prevention/</link>
		<comments>http://www.yourdoctorinfo.com/complete-information-on-autoimmune-inner-ear-disease-with-treatment-and-prevention/#comments</comments>
		<pubDate>Tue, 04 May 2010 13:23:47 +0000</pubDate>
		<dc:creator>Sam</dc:creator>
				<category><![CDATA[Rare Diseases]]></category>
		<category><![CDATA[Autoimmune]]></category>
		<category><![CDATA[Complete]]></category>
		<category><![CDATA[Disease]]></category>
		<category><![CDATA[Information]]></category>
		<category><![CDATA[Inner]]></category>
		<category><![CDATA[Prevention]]></category>
		<category><![CDATA[Treatment]]></category>

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		<description><![CDATA[<p>Auto+immune interior ear illness (AIED) is an incendiary compound circumstance of the interior ear. The reason assumed usually AIED either Antik&amp; #xF6; more rper or it releases cells that Sch&amp; #xE4; digungen the interior ear to induce to be referred. There are references that genetically steered aspects of the immune system erh&amp; #xF6; hen can or otherwise with one erh&amp; #xF6; hten Anf&amp; #xE4; lligkeit f&amp; #xFC; r h&amp; #xE4; ufige H&amp; #xF6; rst&amp; #xF6; rungen such as M&amp; #xE9; ni&amp; #xE8; res illness accompany. It seems that allergies cause k&amp; #xF6; nnen or at least with autoimmune interior ear illnesses. Observation suggests, gives it a genetic component, like autoimmune illnesses, cluster seems in families. Interestingly enough k&amp; #xF6; nnen this characteristic are it shown as different autoimmune illnesses within the same family. However this genetic assessment does not mean alone in addition f&amp; #xFC; hren to develop autoimmune illnesses. Other factors available its m&amp; #xFC; ssen to initiate as well as around the illness. Auto+immune interior ear illness is less a rare illness with than a per cent of the 28 million American with a H&amp; #xF6; rverlust. Both allergies and autoimmune illnesses traditional like disease Bechterew, systemic Lupus of erythematodes, Sjoegren syndrome, k&amp; #xF6; nnen Cogan illness, Colitis ulcerosa, Wegener Granulomatose, rheumatoide Arthritis, Sklerodermie and to be caused or with AIED assigned. The condition to be suggested h&amp; #xE4; more ufiger with female patients, or also simultaneous systemic autoimmune illness can have, than with m&amp; #xE4; nnlichen patients. Autoimmunit&amp; #xE4; t steps with the loss hom&amp; #xF6; ostatischen control of the immune system. Host fabric are recognized as strange and f&amp; #xFC; hren to Besch&amp; #xE4; digungen Vaskulitis and Fibrose. Veldman described a continuum of Autoimmunit&amp; #xE4; t. At an end to produce organ-specific answers with organ-specific Autoantik&amp; #xF6; more rper and T-cells fabric Ver&amp; #xE4; nderung. The symptoms of autoimmune illnesses interior ear illness are abrupt departure Geh&amp; #xF6; r on an ear so fast advance, around the second ear. The Anh&amp; #xF6; rung takeoff can &amp; #xFC; ber weeks or months in advance. Vestibul&amp; #xE4; rer role can allm&amp; #xE4; hlich, so that intensive symptoms do not happen, but patients lost k&amp; #xF6; nnen ataxia and uncertainty still more clearly in the dark with long-term, multilateral vestibul&amp; #xE4; ren subfunction produce. More experience with the illness has this reveals rare findings, and it is not as a routine in the occurrence of the syndrome. Au&amp; #xDF; enohr symptoms, the allergy zur&amp; #xFC; ckgef&amp; #xFC; are hrt k&amp; #xF6; nnen, cover chronic itching or h&amp; #xE4; ufigen infections of the Geh&amp; #xF6; rgangs. Meniere illness in one or both ears occasionally by allergies aggravate. Diagnosis of autoimmune illness interior ear is difficult and often becomes f&amp; #xFC; r Otitis media err, to the patient develop a loss in the second Ohr.Es give different minutes f&amp; #xFC; r the treatment of autoimmune illness interior ear. Therapy goals into auto+immune illness interior ear geh&amp; #xF6; ren the improvement of the speech threshold values levels treatable with H&amp; #xF6; rger&amp; #xE4; ten with patients heavily concerned and the utilization of the H&amp; #xF6; rens in the N&amp; #xE4; a he normal level with the patients with easier to moderately severe losses. Most patients with autoimmune illness interior ear on the Erstbehandlung of Steroiden to react to Prednison and Methotrexat, a chemotherapeutic agent. Some patients k&amp; #xF6; nnen by the use of H&amp; #xF6; rger&amp; #xE4; ten profit. With persons with reaction to Steroide, into most F&amp; #xE4; llen a chemotherapy kind of medicines such as Cytoxan or one will on a long-term basis use. The medicine can directly into the interior ear under &amp; #xF6; rtlicher Bet&amp; #xE4; ubung, or by the use of tiny R&amp; #xF6; hrchen in the ear eingef&amp; #xFC; hrt to be placed by surgery. Not all humans react to the therapy Steroid the same way. Treatment with some humans f&amp; #xFC; hrt to a better H&amp; #xF6; ren, or better discrimination or both.  <a href='http://www.yourdoctorinfo.com/complete-information-on-autoimmune-inner-ear-disease-with-treatment-and-prevention/' rel="nofollow">Read More</a></p>]]></description>
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		<title>Kawasaki Disease- A Rare Disease In Infants</title>
		<link>http://www.yourdoctorinfo.com/kawasaki-disease-a-rare-disease-in-infants/</link>
		<comments>http://www.yourdoctorinfo.com/kawasaki-disease-a-rare-disease-in-infants/#comments</comments>
		<pubDate>Thu, 29 Apr 2010 13:22:23 +0000</pubDate>
		<dc:creator>Sam</dc:creator>
				<category><![CDATA[Rare Diseases]]></category>
		<category><![CDATA[Disease]]></category>
		<category><![CDATA[Infants]]></category>
		<category><![CDATA[Kawasaki]]></category>
		<category><![CDATA[rare]]></category>

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		<description><![CDATA[<p>The message of Jetta Travolta, son of John Travolta and Kelly Peterson died pl&amp; #xF6; tzlich after an accumulation suffers, w&amp; #xE4; it in the vacation was hrend with its family in the Bahamas. It was diagnosed with Kawasaki syndrome, when it was straight 15 months old. Brian suffering ral Backstreet Boys fame k&amp; #xFC; ndigte also its son Baylee with Kawasaki syndrome is made a diagnosis. Kawasaki illness: It is an illness to get the young children for more in medical regard more acutely selflimited immune-conciliatory form of the Vaskulitis, those above all S&amp; #xE4; uglinge and infants. Kawasaki illness, those primarily S&amp; #xE4; uglinge and small children, is by pl&amp; #xF6; tzliches using of fever, skin excursion marked and Vaskulitis.Symptome and indication children by Kawasaki illness knows a multiplicity of different symptoms up: Pl&amp; #xF6; tzliche occurrence of Fieber&amp; #xDC; belkeitErbrechenErkrankung the GallenblaseBindehautentz&amp; #xFC; ndung, both the Augenger&amp; #xF6; teten lips and MundschleimhautHautausschl&amp; #xE4; geerweiterten themselves HalslymphknotenUnd knows even Arthritis.Die a cause Kawasaki illness is unknown, but if the symptoms fr&amp; #xFC; hzeitig to be recognized, k&amp; #xF6; nnen children with Kawasaki illness vollst&amp; #xE4; recover ndig within a few days. Untreatedly it can to serious complications such as lead: Aneurysms of the KoronararterienHerzinfarkteIsch&amp; #xE4; mix HerzkrankheitKoronarer Thrombose (Blutgerinnsel) Kawasaki illness is h&amp; #xE4; ufigste a cause of heart illnesses with Kindern.Hautausschl&amp; #xE4; ge of the Kawasaki illness: The excursion in Kawasaki illness, different forms have, but to h&amp; #xE4; ufigsten form are a nonspecific, diffuse, outbreak of the flattened Papeln. The Ausschl&amp; #xE4; ge on the entire K&amp; #xF6; more rper, einschlie&amp; #xDF; lich the trunk and the Extremit&amp; #xE4; ten and also itching. One ger&amp; #xF6; tete &quot; Erdbeere&quot; Tongue can likewise occur. Causes and DiagnoseDie causes of the Kawasaki illness remains verbl&amp; #xFC; ffend. Specific exciters in Kawasaki illness, but one was not identified infekti&amp; #xF6; SE Ausl&amp; #xF6; more ser assumes. There are no specific diagnostic tests to the Verf&amp; #xFC; gung. Kawasaki illness is assumed, if the characteristic signs and symptoms present with small child complication with diagnosis: One unvollst&amp; #xE4; ndige form of the Kawasaki illness, ith e. Only few of the characteristic symptoms and from there makes difficult it arises to differentiate of viralen as well as Staphylococcus and Sreptococcus infections. Also in the past Kawasaki syndrome became as Periarteriitis with reports of old F&amp; #xE4; llen appear identical t&amp; #xF6; dliche F&amp; #xE4; lle of Kawasaki illness today were falsediagnosed. To complications also arise, if the symptoms show up, at different times, sometimes do not arise, until first pl&amp; #xF6; tzliche occurrence of symptoms seems gel&amp; #xF6; to be st. Treatment: The treatment consists of aspirin therapy and intraven&amp; #xF6; ses Immunglobulin therapy.  <a href='http://www.yourdoctorinfo.com/kawasaki-disease-a-rare-disease-in-infants/' rel="nofollow">Read More</a></p>]]></description>
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		</item>
		<item>
		<title>MRI With Contrast Dye Can Cause Rare Disease</title>
		<link>http://www.yourdoctorinfo.com/mri-with-contrast-dye-can-cause-rare-disease/</link>
		<comments>http://www.yourdoctorinfo.com/mri-with-contrast-dye-can-cause-rare-disease/#comments</comments>
		<pubDate>Sat, 24 Apr 2010 13:22:45 +0000</pubDate>
		<dc:creator>Sam</dc:creator>
				<category><![CDATA[Rare Diseases]]></category>
		<category><![CDATA[Cause]]></category>
		<category><![CDATA[Contrast]]></category>
		<category><![CDATA[Disease]]></category>
		<category><![CDATA[rare]]></category>

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		<description><![CDATA[<p>              Gadolinium injection used to get a better MRI image can cause a rare disease known as nephrogenic fibrosing dermopathy (NFD) or nephrogenic systemic fibrosis (NSF) in people with kidney problems. &#xD;NFD/NSF: What Are The Symptoms?&#xD;Patients with NSF describe swelling and tightening of the skin, usually limited to the arms and legs but sometimes involving the trunk of the body.  The condition may develop over a period of days to several weeks.  In many cases, the skin thickening inhibits the movement of the joints, resulting in a condition where the joint is bent and will not move.   Severely affected patients may be unable to walk, or fully extend the joints of their arms, hands, legs, and feet.  Complaints of muscle weakness are common.  Approximately 5% of patients have a rapidly progressive course. &#xD;The skin changes may start as reddened or darkened patches or bumps.  In time, the skin may feel &#8220;woody&#8221; and the surface may resemble the texture of the peel of an orange.  Patients may experience burning, itching, or severe sharp pains in areas of involvement.   Deep &#8220;bone pain&#8221; has been described in the hips and in the ribs. &#xD;The skin injuries are commonly symmetrical, with zones between the ankles and thighs most commonly involved, followed by involvement between the wrist and upper arms.  Hand and foot swelling with blister-like damage has also been reported.  Some patients have reported yellow bumps or patches on or near the eyes.  Rapid, new onset fluctuating high blood pressure of unknown cause has been described prior to the onset of the skin damage. &#xD;(From The International Center for Nephrogenic Fibrosing Dermopathy Research. )&#xD;NFD/NSF: What Are The Treatment options?&#xD;While there is no consistently successful treatment for NSF, improving renal function (due to any modality) seems to slow or arrest NSF (and in many cases allows for gradual reversal of the process over time). &#xD;Critical assessment of the effects of any investigational therapy requires careful attention *and reporting* of the patient&#8217;s renal function during therapy.  Investigational therapies that show objective improvement in the setting of worsening or stable chronic renal failure should be targeted for further investigation.  Therapies that show improvement of NSF while renal function is improving may or may not be contributing to the observed improvement.  Given the recent association of NSF with gadolinium administration, any reports of investigational therapies should also clearly indicate whether gadolinium was administered during the therapeutic evaluation, and whether there was an identifiable clinical change in the patient&#8217;s disease. &#xD;Treatments that have been tried and continue to be investigated include:&#xD;Oral steroids (prednisone): Patients with concurrent diabetes should be aware of the risks of hyperglycemia while taking this medication.  All patients should be aware of the possibility of gastrointestinal ulceration while taking prednisone.  In addition, osteoporosis is often accelerated while taking this medication. &#xD;Topical Dovonex (Dovonex is an ointment approved by the FDA for treating psoriasis) : So far, responses have been anecdotal and largely subjective.  Some patients report improvement in localized disease. &#xD;Extracorporeal photopheresis (ECP): (Note: the patient is given certain drugs which are sensitive to the influence of light then the patients blood is run through a device outside the body [extracorporeal] during which the blood is subjected to ultraviolet rays. ) A recent article describes three patients in Europe who responded with softening of plaques after several courses of ECP.  Each of these patients had no improvement in renal function during the treatment.  All three of these patients had had NSF for less than one year.  Experience at Yale suggests that patients with longstanding NSF (arbitrarily set at one year) may not respond to this modality.  This treatment is currently under investigation, although no formal trials are yet offered.  Some insurance carriers are receptive to covering a trial of therapy, but in the event coverage cannot be secured, be advised that therapy is exceedingly expensive.  Many patients and providers have reported that Medicare has provided coverage for ECP in recent cases. &#xD;Plasmapheresis: (this is a blood purification procedure which removes antibodies from the blood) As with photopheresis this treatment method is extracorporeal meaning the blood is routed out of the body, treated, and then routed back to the body.  One study from Loma Linda University (ref 12) reported improvement in three patients with liver/kidney transplant.  Two of these patients were noted to have concurrent improving renal function.  It is unclear what contribution improving renal function may have had in the overall clinical improvement.  Nevertheless, anecdotally, some persons have reported slight improvement following plasmapheresis.  Several others have been reported who noted no improvement at all. &#xD;Cytoxan: (this drug is normally used in chemotherapy to treat cancer) Anecdotally, this medication has shown no improvement in a number of NSF patients. &#xD;Thalidomide: (Thalidomide was first marketed in the 1950s and a sleeping pill and as a treatment for morning sickness.  It is now believed to cause birth defects and so is not approved for sale in the U. S.  but the FDA allows its usage in certain studied.  ) There are no formal reports on the success of this medication in NSF.  However, some patients have reported subjective improvement.  Long term tolerance of the drug may be an issue, however.  . &#xD;Ultraviolet therapy: Some anecdotal use but no reports of success. &#xD;Physical therapy (PT): Some patients have reported that physical therapy, in particular, swimming, may be helpful in slowing the progression of joint contractures.  (Contractures are joints that are bent but unmovable from scar tissue formation. ) There is no contraindication to PT, and the definite potential up-side suggests that PT should be pursued whenever possible.  Deep massage has been reported to be of benefit. &#xD;Pentoxifylline (PXF): ( This medication which is also known as Trental decreases the &#8220;stickiness&#8221; (viscosity) of blood and thereby improves its flow.  This increased blood flow helps patients with peripheral arterial disease to obtain better circulation and oxygen delivery to vital tissues.  It is used to treat a condition of painful legs that develop with exercise because of inadequate circulation to the legs and feet)  A recent report describes two NSF patients who received 1200 mg per day of oral pentoxifylline .  Both patients stabilized, and the one with less severe disease improved somewhat.  As thrombosis (blood clotting) seems to be an inciting event for many NSF patients, this mechanism could also be partially responsible for the improvements noted clinically.  Many more patients will need to be treated to further evaluate the efficacy of this drug. &#xD;High Dose Intravenous Ig (Immunoglobulin) Therapy: (Immunoglobulins are antibodies found in the human body) One patient showed objective improvements with one cycle of therapy with this medication.  Further improvement with additional cycles was not observed.  No comment was made regarding the renal status of the patient while receiving this therapy.   There is anecdotal information suggesting this therapy has been helpful in one other patient with NSF.  Additional anecdotal data have been less promising. &#xD;Kidney transplant: Several patients have improved significantly with a return to normal kidney function (either as a result of transplantation or medical therapy).  In other cases, kidney transplant has resulted in no obvious improvement of the lesions, even with a fully functioning, successfully transplanted organ.             <a href='http://www.yourdoctorinfo.com/mri-with-contrast-dye-can-cause-rare-disease/' rel="nofollow">Read More</a></p>]]></description>
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		<item>
		<title>AN OVERVIEW ON PROGERIA: A RARE DISEASE OF CHILD</title>
		<link>http://www.yourdoctorinfo.com/an-overview-on-progeria-a-rare-disease-of-child/</link>
		<comments>http://www.yourdoctorinfo.com/an-overview-on-progeria-a-rare-disease-of-child/#comments</comments>
		<pubDate>Mon, 19 Apr 2010 13:24:17 +0000</pubDate>
		<dc:creator>Sam</dc:creator>
				<category><![CDATA[Rare Diseases]]></category>
		<category><![CDATA[Child]]></category>
		<category><![CDATA[Disease]]></category>
		<category><![CDATA[Overview]]></category>
		<category><![CDATA[PROGERIA]]></category>
		<category><![CDATA[rare]]></category>

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		<description><![CDATA[<p><strong>AN OVERVIEW ON PROGERIA: A RARE DISEASE OF CHILD </strong> <a href='http://www.yourdoctorinfo.com/an-overview-on-progeria-a-rare-disease-of-child/' rel="nofollow">Read More</a></p>]]></description>
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		<item>
		<title>Babesia: Rare Disease Not So Rare</title>
		<link>http://www.yourdoctorinfo.com/babesia-rare-disease-not-so-rare/</link>
		<comments>http://www.yourdoctorinfo.com/babesia-rare-disease-not-so-rare/#comments</comments>
		<pubDate>Mon, 19 Apr 2010 13:23:19 +0000</pubDate>
		<dc:creator>Sam</dc:creator>
				<category><![CDATA[Rare Diseases]]></category>
		<category><![CDATA[Babesia]]></category>
		<category><![CDATA[Disease]]></category>
		<category><![CDATA[rare]]></category>

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		<description><![CDATA[<p>Until recently, Babesia was considered a rare disease because it was only diagnosed in extremely ill patients with high fevers (104+).  The bacteria which invades the red blood cells, has been largely ignored by the medical community in part because there wasn&#8217;t a reliable test for diagnosing it, and in part because there has been so little information about the disease. <a href='http://www.yourdoctorinfo.com/babesia-rare-disease-not-so-rare/' rel="nofollow">Read More</a></p>]]></description>
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