<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?action=history&amp;feed=atom&amp;title=Leber%E2%80%99s_hereditary_optic_neuropathy_%28LHON%29</id>
	<title>Leber’s hereditary optic neuropathy (LHON) - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?action=history&amp;feed=atom&amp;title=Leber%E2%80%99s_hereditary_optic_neuropathy_%28LHON%29"/>
	<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Leber%E2%80%99s_hereditary_optic_neuropathy_(LHON)&amp;action=history"/>
	<updated>2026-04-15T05:44:24Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
	<generator>MediaWiki 1.44.0</generator>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Leber%E2%80%99s_hereditary_optic_neuropathy_(LHON)&amp;diff=23116&amp;oldid=prev</id>
		<title>180038248: Created page with &quot;&amp;nbsp;   = Leber&#039;s hereditary optic neuropathy (LHON)  =  LHON is a form of vision loss and it is a result of atrophy of the optic nerve, the nerve that transmits...&quot;</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Leber%E2%80%99s_hereditary_optic_neuropathy_(LHON)&amp;diff=23116&amp;oldid=prev"/>
		<updated>2018-12-06T20:32:46Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;    = Leber&amp;#039;s hereditary optic neuropathy (LHON)  =  LHON is a form of vision loss and it is a result of atrophy of the &lt;a href=&quot;/bms/wiki//index.php?title=Optic_nerve&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Optic nerve (page does not exist)&quot;&gt;optic nerve&lt;/a&gt;, the nerve that transmits...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;amp;nbsp; &lt;br /&gt;
&lt;br /&gt;
= Leber&amp;#039;s hereditary optic neuropathy (LHON)  =&lt;br /&gt;
&lt;br /&gt;
LHON is a form of vision loss and it is a result of atrophy of the [[Optic nerve|optic nerve]], the nerve that transmits messages containing visual information from the eyes to the brain. LHON is a [[Mitochondrial disease|mitochondrial disease]] in which mutations occur in&amp;amp;nbsp;the MT-ND1, MT-ND4, MT-ND4L, and MT-ND6 [[Genes|genes]].&amp;lt;ref&amp;gt;This is a reference to the website of &amp;quot;National Centre for Advancing Translational Science&amp;quot;, &amp;quot;Genetic and Rare diseases Information Centre&amp;quot; section.&amp;lt;/ref&amp;gt;&amp;amp;nbsp;It is a disease that affects young adults, predominantly males (very unlikely for LHON to appear in childhood). The vision loss may start in one eye or both eyes at the same time. &amp;amp;nbsp;As the disease progress, the individual will lose his ability to read, drive and recognizing faces.&amp;amp;nbsp;&amp;lt;ref&amp;gt;This is a reference to the website of &amp;quot;U.S. National Library of Medicine&amp;quot;- Genetic Home Reference&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
== &amp;amp;nbsp;LHON plus  ==&lt;br /&gt;
&lt;br /&gt;
LHON puls has some additional features besides the vision loss such as: the incapability of doing certain movements, tremor and [[Heart arrhythmias|heart arrhythmias]]. These features are similar to [[Multiple sclerosis|multiple sclerosis]], a chronic disorder.&amp;lt;ref&amp;gt;This is a reference to the website of &amp;quot;National Centre for Biotechnology Information (NCBI)&amp;quot;&amp;lt;/ref&amp;gt;&amp;amp;nbsp;Currently, there is no cure for this disease. Further reseach needs to be made in order for us to obtain a better understanding of LHON.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
== &amp;lt;span style=&amp;quot;font-size: 19.920000076293945px;&amp;quot;&amp;gt;References&amp;lt;/span&amp;gt;  ==&lt;br /&gt;
&lt;br /&gt;
&amp;amp;lt;span style=&amp;quot;font-size: 19.920000076293945px;&amp;quot; /&amp;amp;gt;&amp;lt;references /&amp;gt;&lt;/div&gt;</summary>
		<author><name>180038248</name></author>
	</entry>
</feed>