<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[RSS Feed]]></title><description><![CDATA[RSS Feed]]></description><link>http://direct.ecency.com</link><image><url>http://direct.ecency.com/logo512.png</url><title>RSS Feed</title><link>http://direct.ecency.com</link></image><generator>RSS for Node</generator><lastBuildDate>Sun, 12 Apr 2026 17:52:09 GMT</lastBuildDate><atom:link href="http://direct.ecency.com/@karthikmbbs2/rss" rel="self" type="application/rss+xml"/><item><title><![CDATA[Leclanche cell]]></title><description><![CDATA[Leclanche cell A Leclanche cell consists of a carbon electrode packed in a porous pot containing manganese dioxide and charcoal powder. The porous pot is immersed in a saturated solution of ammonium chloride]]></description><link>http://direct.ecency.com/steemstem/@karthikmbbs2/leclanche-cell-667a20a11da5a</link><guid isPermaLink="true">http://direct.ecency.com/steemstem/@karthikmbbs2/leclanche-cell-667a20a11da5a</guid><category><![CDATA[steemstem]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Sun, 10 Jun 2018 07:22:51 GMT</pubDate><enclosure url="https://images.ecency.com/p/o1AJ9qDyyJNSpZWhUgGYc3MngFqoAN4KzX7fgpMgPHBhEqf26?format=match&amp;mode=fit" length="0" type="false"/></item><item><title><![CDATA[Majeed Syndrome]]></title><description><![CDATA[It is an inherited skin disorder characterized by chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and a neutrophilic dermatosis.[1] It is classified as an autoinflammatory]]></description><link>http://direct.ecency.com/steempress/@karthikmbbs2/majeedsyndrome-kte755sims</link><guid isPermaLink="true">http://direct.ecency.com/steempress/@karthikmbbs2/majeedsyndrome-kte755sims</guid><category><![CDATA[steempress]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Thu, 07 Jun 2018 14:05:18 GMT</pubDate></item><item><title><![CDATA[Ardalan–Shoja–Kiuru syndrome]]></title><description><![CDATA[Ardalan–Shoja–Kiuru syndrome is a clinical syndrome featuring hereditary gelsolin [1] amyloidosis and retinitis pigmentosa.[2] This syndrome was first recognized by two Iranian physicians, Mohammad Ardalan]]></description><link>http://direct.ecency.com/ardalanshojakiuru/@karthikmbbs2/ardalan-shoja-kiuru-syndrome-919d10168e637</link><guid isPermaLink="true">http://direct.ecency.com/ardalanshojakiuru/@karthikmbbs2/ardalan-shoja-kiuru-syndrome-919d10168e637</guid><category><![CDATA[ardalanshojakiuru]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Mon, 04 Jun 2018 17:53:36 GMT</pubDate></item><item><title><![CDATA[Anticonvulsant/sulfonamide hypersensitivity syndrome]]></title><description><![CDATA[Anticonvulsant/sulfonamide hypersensitivity syndrome is a potentially serious hypersensitivity reaction that can be seen with drugs with an aromatic amine chemical structure, such as aromatic anticonvulsants]]></description><link>http://direct.ecency.com/anticonvulsantsulfonamide/@karthikmbbs2/anticonvulsant-sulfonamide-hypersensitivity-syndrome-1703af3757178</link><guid isPermaLink="true">http://direct.ecency.com/anticonvulsantsulfonamide/@karthikmbbs2/anticonvulsant-sulfonamide-hypersensitivity-syndrome-1703af3757178</guid><category><![CDATA[anticonvulsantsulfonamide]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Fri, 01 Jun 2018 15:44:27 GMT</pubDate></item><item><title><![CDATA[Amplified musculoskeletal pain syndromes]]></title><description><![CDATA[Amplified musculoskeletal pain syndromes are pain syndromes where excessive, acute and chronic pain are observed for which no overt primary cause can be found or surmised.[1] Amplified musculoskeletal]]></description><link>http://direct.ecency.com/vincentb/@karthikmbbs2/amplified-musculoskeletal-pain-syndromes-0cab74abe3a35</link><guid isPermaLink="true">http://direct.ecency.com/vincentb/@karthikmbbs2/amplified-musculoskeletal-pain-syndromes-0cab74abe3a35</guid><category><![CDATA[vincentb]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Wed, 30 May 2018 15:44:06 GMT</pubDate></item><item><title><![CDATA[Todays thought]]></title><description><![CDATA[Thanks for reading.. Have a great day..]]></description><link>http://direct.ecency.com/thought/@karthikmbbs2/todays-thought-d2bb4e0309fcd</link><guid isPermaLink="true">http://direct.ecency.com/thought/@karthikmbbs2/todays-thought-d2bb4e0309fcd</guid><category><![CDATA[thought]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Mon, 28 May 2018 05:28:21 GMT</pubDate><enclosure url="https://images.ecency.com/p/o1AJ9qDyyJNSpZWhUgGYc3MngFqoAMx5u9B26FZKLd65kaJia?format=match&amp;mode=fit" length="0" type="false"/></item><item><title><![CDATA[Al-Raqad syndrome]]></title><description><![CDATA[Al-Raqad syndrome (ARS) is a congenital autosomal recessive syndrome discovered by Jordanian physician Mohammad Al-Raqad. It's characterized by: microcephaly growth delay Psycho-motor developmental delay]]></description><link>http://direct.ecency.com/al-raqad/@karthikmbbs2/al-raqad-syndrome-e4721765da9bd</link><guid isPermaLink="true">http://direct.ecency.com/al-raqad/@karthikmbbs2/al-raqad-syndrome-e4721765da9bd</guid><category><![CDATA[al-raqad]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Fri, 25 May 2018 16:19:48 GMT</pubDate></item><item><title><![CDATA[Aicardi–Goutières syndrome]]></title><description><![CDATA[Aicardi–Goutières syndrome (AGS), which is completely distinct from the similarly named Aicardi syndrome, is a rare, usually early onset childhood, inflammatory disorder most typically affecting the brain]]></description><link>http://direct.ecency.com/aicardigoutires/@karthikmbbs2/aicardi-goutieres-syndrome-135b232d9258f</link><guid isPermaLink="true">http://direct.ecency.com/aicardigoutires/@karthikmbbs2/aicardi-goutieres-syndrome-135b232d9258f</guid><category><![CDATA[aicardigoutires]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Wed, 23 May 2018 19:03:57 GMT</pubDate></item><item><title><![CDATA[Adie syndrome]]></title><description><![CDATA[Adie syndrome is a neurological disorder characterized by a tonically dilated pupil that reacts slowly to light but shows a more definite response to accommodation (i.e., light-near dissociation).[1] It]]></description><link>http://direct.ecency.com/adie/@karthikmbbs2/adie-syndrome-8af901672a5be</link><guid isPermaLink="true">http://direct.ecency.com/adie/@karthikmbbs2/adie-syndrome-8af901672a5be</guid><category><![CDATA[adie]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Tue, 22 May 2018 15:31:36 GMT</pubDate></item><item><title><![CDATA[Adams–Nance syndrome]]></title><description><![CDATA[Adams–Nance syndrome is a medical condition consisting of persistent tachycardia, paroxymal hypertension and seizures. It is associated with hyperglycinuria, dominantly inherited microphthalmia and cataracts.]]></description><link>http://direct.ecency.com/adamsnance/@karthikmbbs2/adams-nance-syndrome-e7aec6cdbd57f</link><guid isPermaLink="true">http://direct.ecency.com/adamsnance/@karthikmbbs2/adams-nance-syndrome-e7aec6cdbd57f</guid><category><![CDATA[adamsnance]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Mon, 21 May 2018 17:55:48 GMT</pubDate></item><item><title><![CDATA[Acute motor axonal neuropathy]]></title><description><![CDATA[Acute motor axonal neuropathy (AMAN) is a variant of Guillain–Barré syndrome. It is characterized by acute paralysis and loss of reflexes without sensory loss. Pathologically, there is motor axonal]]></description><link>http://direct.ecency.com/acute/@karthikmbbs2/acute-motor-axonal-neuropathy-d91fc5ff75536</link><guid isPermaLink="true">http://direct.ecency.com/acute/@karthikmbbs2/acute-motor-axonal-neuropathy-d91fc5ff75536</guid><category><![CDATA[acute]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Sat, 19 May 2018 15:08:03 GMT</pubDate></item><item><title><![CDATA[Acute hepatomyoencephalopathy (HME) syndrome]]></title><description><![CDATA[Acute hepatomyoencephalopathy (HME) syndrome is the name given to a multi-system disease affecting the liver, muscle and brain which is now known to be caused by phytotoxins.[1] After extensive investigation]]></description><link>http://direct.ecency.com/acute/@karthikmbbs2/acute-hepatomyoencephalopathy-hme-syndrome-01af5f2270274</link><guid isPermaLink="true">http://direct.ecency.com/acute/@karthikmbbs2/acute-hepatomyoencephalopathy-hme-syndrome-01af5f2270274</guid><category><![CDATA[acute]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Sat, 19 May 2018 14:59:24 GMT</pubDate></item><item><title><![CDATA[acute chest syndrome]]></title><description><![CDATA[The acute chest syndrome is a vaso-occlusive crisis of the pulmonary vasculature commonly seen in people with sickle cell anemia. This condition commonly manifests with a new opacification of the lung(s)]]></description><link>http://direct.ecency.com/acute/@karthikmbbs2/acute-chest-syndrome-91694284deea5</link><guid isPermaLink="true">http://direct.ecency.com/acute/@karthikmbbs2/acute-chest-syndrome-91694284deea5</guid><category><![CDATA[acute]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Thu, 17 May 2018 17:25:54 GMT</pubDate></item><item><title><![CDATA[Activation syndrome]]></title><description><![CDATA[Activation syndrome is a form of stimulation (sometimes suicidal) or agitation that has been observed in association with some psychoactive drugs.[1] A causative role has not been established.[2] Pfizer]]></description><link>http://direct.ecency.com/activation/@karthikmbbs2/activation-syndrome-341956f2e8d7a</link><guid isPermaLink="true">http://direct.ecency.com/activation/@karthikmbbs2/activation-syndrome-341956f2e8d7a</guid><category><![CDATA[activation]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Thu, 17 May 2018 17:19:21 GMT</pubDate></item><item><title><![CDATA[Acro–dermato–ungual–lacrimal–tooth (ADULT) syndrome]]></title><description><![CDATA[Acro–dermato–ungual–lacrimal–tooth (ADULT) syndrome is a rare genetic disease.[1] ADULT syndrome is an autosomal dominant form of ectodermal dysplasia, a group of disorders that affects the hair, teeth,]]></description><link>http://direct.ecency.com/acrodermatounguallacrimaltooth/@karthikmbbs2/acro-dermato-ungual-lacrimal-tooth-adult-syndrome-260c5ebe3d986</link><guid isPermaLink="true">http://direct.ecency.com/acrodermatounguallacrimaltooth/@karthikmbbs2/acro-dermato-ungual-lacrimal-tooth-adult-syndrome-260c5ebe3d986</guid><category><![CDATA[acrodermatounguallacrimaltooth]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Thu, 17 May 2018 17:13:15 GMT</pubDate></item><item><title><![CDATA[Ackerman syndrome]]></title><description><![CDATA[Ackerman syndrome is a familial syndrome of fused molar roots with a single canal (taurodontism), hypotrichosis, full upper lip without a cupid’s bow, thickened and wide philtrum, and occasional juvenile]]></description><link>http://direct.ecency.com/ackerman/@karthikmbbs2/ackerman-syndrome-2e3f590a683c6</link><guid isPermaLink="true">http://direct.ecency.com/ackerman/@karthikmbbs2/ackerman-syndrome-2e3f590a683c6</guid><category><![CDATA[ackerman]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Wed, 16 May 2018 14:16:21 GMT</pubDate></item><item><title><![CDATA[Achard syndrome]]></title><description><![CDATA[Achard syndrome is a syndrome consisting of arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet.[1] Hypermobility and subluxations of the joints, increased lateral excursion]]></description><link>http://direct.ecency.com/achard/@karthikmbbs2/achard-syndrome-db680170617d9</link><guid isPermaLink="true">http://direct.ecency.com/achard/@karthikmbbs2/achard-syndrome-db680170617d9</guid><category><![CDATA[achard]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Wed, 16 May 2018 14:06:51 GMT</pubDate></item><item><title><![CDATA[Ablepharon macrostomia syndrome]]></title><description><![CDATA[Ablepharon macrostomia syndrome (AMS) is an extremely rare autosomal recessive genetic disorder characterized by malformations of the skull, skin, fingers and genitals.[1] Affected individuals may also]]></description><link>http://direct.ecency.com/ablepharon/@karthikmbbs2/ablepharon-macrostomia-syndrome-ef3d56c92c56c</link><guid isPermaLink="true">http://direct.ecency.com/ablepharon/@karthikmbbs2/ablepharon-macrostomia-syndrome-ef3d56c92c56c</guid><category><![CDATA[ablepharon]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Tue, 15 May 2018 17:45:54 GMT</pubDate></item><item><title><![CDATA[Abderhalden–Kaufmann–Lignac syndrome]]></title><description><![CDATA[Abderhalden–Kaufmann–Lignac syndrome (AKL syndrome), also called nephropathic cystinosis, is an autosomal recessive renal disorder of childhood comprising cystinosis and renal rickets.]]></description><link>http://direct.ecency.com/abderhaldenkaufmannlignac/@karthikmbbs2/abderhalden-kaufmann-lignac-syndrome-7eeb6574e8033</link><guid isPermaLink="true">http://direct.ecency.com/abderhaldenkaufmannlignac/@karthikmbbs2/abderhalden-kaufmann-lignac-syndrome-7eeb6574e8033</guid><category><![CDATA[abderhaldenkaufmannlignac]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Tue, 15 May 2018 17:39:57 GMT</pubDate></item><item><title><![CDATA[Abandoned child syndrome]]></title><description><![CDATA[Abandoned child syndrome is a behavioral or psychological condition that results primarily from the loss of one or both parents, or sexual abuse. Abandonment may be physical (the parent is not present]]></description><link>http://direct.ecency.com/abandoned/@karthikmbbs2/abandoned-child-syndrome-d51187df27534</link><guid isPermaLink="true">http://direct.ecency.com/abandoned/@karthikmbbs2/abandoned-child-syndrome-d51187df27534</guid><category><![CDATA[abandoned]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Mon, 14 May 2018 16:54:39 GMT</pubDate></item></channel></rss>