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	<id>https://librepathology.org/w/index.php?action=history&amp;feed=atom&amp;title=Adrenoleukodystrophy</id>
	<title>Adrenoleukodystrophy - Revision history</title>
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	<updated>2026-06-16T02:41:41Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://librepathology.org/w/index.php?title=Adrenoleukodystrophy&amp;diff=16530&amp;oldid=prev</id>
		<title>Michael: create</title>
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		<updated>2012-05-31T02:55:01Z</updated>

		<summary type="html">&lt;p&gt;create&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;'''Adrenoleukodystrophy''' a rare genetic disorder.  It is classically described as X-linked with onset in childhood.&amp;lt;ref name=omim300100&amp;gt;{{OMIM|300100}}&amp;lt;/ref&amp;gt; An autosomal neonatal form also exists.&amp;lt;ref name=omim202370&amp;gt;{{OMIM|202370}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==General==&lt;br /&gt;
Clinical:&lt;br /&gt;
*Increased serum long-chain fatty acid levels.&amp;lt;ref name=pmid21871076&amp;gt;{{Cite journal  | last1 = Terre'Blanche | first1 = G. | last2 = van der Walt | first2 = MM. | last3 = Bergh | first3 = JJ. | last4 = Mienie | first4 = LJ. | title = Treatment of an adrenomyeloneuropathy patient with Lorenzo's oil and supplementation with docosahexaenoic acid--a case report. | journal = Lipids Health Dis | volume = 10 | issue =  | pages = 152 | month =  | year = 2011 | doi = 10.1186/1476-511X-10-152 | PMID = 21871076 }}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
*[[Addison disease]].&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist|1}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Neuropathology]]&lt;br /&gt;
[[Category:Adrenal gland]]&lt;br /&gt;
[[Category:Pediatric pathology]]&lt;/div&gt;</summary>
		<author><name>Michael</name></author>
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