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	<title>File:Friedreich's Ataxia Pedigree.png - Revision history</title>
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	<updated>2026-10-23T14:52:22Z</updated>
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		<title>Z3389343: The pedigree of a family affected by Friedreich's Ataxia. Due to the anticipating nature of the inheritance, the severity of symptoms increases while the age of onset decreases with each generation. Heterozygous individuals who possess one allele with the</title>
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		<updated>2011-10-10T06:42:47Z</updated>

		<summary type="html">&lt;p&gt;The pedigree of a family affected by Friedreich&amp;#039;s Ataxia. Due to the anticipating nature of the inheritance, the severity of symptoms increases while the age of onset decreases with each generation. Heterozygous individuals who possess one allele with the&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;The pedigree of a family affected by Friedreich's Ataxia. Due to the anticipating nature of the inheritance, the severity of symptoms increases while the age of onset decreases with each generation. Heterozygous individuals who possess one allele with the repeat expansion do not develop symptoms, and are thus unaffected carriers. The expression of Friedreich's Ataxia occurs only when an individual carries two mutated frataxin alleles.&lt;br /&gt;
Please note that this pedigree is entirely fictional and solely serves as a model to illustrate the mode of inheritance.&lt;br /&gt;
&lt;br /&gt;
'''Copyright''' Beginning six months after publication, I (z3389343) grant the public the non-exclusive right to copy, distribute, or display the Work under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/ and http://creativecommons.org/licenses/by-nc-sa/3.0/legalcode&lt;br /&gt;
&lt;br /&gt;
Drawn by student z3389343.&lt;br /&gt;
&lt;br /&gt;
{{Template:2011 Student Image}}&lt;/div&gt;</summary>
		<author><name>Z3389343</name></author>
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