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	<title>Contiguous gene syndrome - Revision history</title>
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	<updated>2026-04-23T22:39:27Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.com/index.php?title=Contiguous_gene_syndrome&amp;diff=6501972&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2025-03-17T07:57:07Z</updated>

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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 07:57, 17 March 2025&lt;/td&gt;
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		<author><name>Prab</name></author>
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	<entry>
		<id>https://wikimd.com/index.php?title=Contiguous_gene_syndrome&amp;diff=6221592&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2025-02-10T12:13:59Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 12:13, 10 February 2025&lt;/td&gt;
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		<author><name>Prab</name></author>
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	<entry>
		<id>https://wikimd.com/index.php?title=Contiguous_gene_syndrome&amp;diff=5169557&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.com/index.php?title=Contiguous_gene_syndrome&amp;diff=5169557&amp;oldid=prev"/>
		<updated>2024-02-20T05:59:31Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Contiguous gene syndrome&amp;#039;&amp;#039;&amp;#039; is a medical condition that occurs when a deletion or duplication in a person&amp;#039;s DNA affects multiple genes that are located close to each other on the same chromosome. This syndrome is characterized by a wide range of symptoms, which can vary greatly from person to person depending on the specific genes that are affected.&lt;br /&gt;
&lt;br /&gt;
== Causes ==&lt;br /&gt;
&lt;br /&gt;
Contiguous gene syndrome is caused by a deletion or duplication of a segment of DNA that includes multiple genes. This can occur as a random event during the formation of reproductive cells (eggs or sperm) or in early fetal development. In some cases, the syndrome can be inherited from a parent who carries a chromosomal rearrangement such as a translocation.&lt;br /&gt;
&lt;br /&gt;
== Symptoms ==&lt;br /&gt;
&lt;br /&gt;
The symptoms of contiguous gene syndrome can vary greatly depending on the specific genes that are affected. Some people may have physical abnormalities, intellectual disability, or health problems such as heart disease or cancer. Others may have no noticeable symptoms.&lt;br /&gt;
&lt;br /&gt;
== Diagnosis ==&lt;br /&gt;
&lt;br /&gt;
Diagnosis of contiguous gene syndrome typically involves genetic testing to identify the specific deletion or duplication. This can include karyotyping, which provides a broad overview of a person&amp;#039;s chromosomes, or more detailed tests such as microarray analysis or next-generation sequencing.&lt;br /&gt;
&lt;br /&gt;
== Treatment ==&lt;br /&gt;
&lt;br /&gt;
There is currently no cure for contiguous gene syndrome. Treatment typically focuses on managing the symptoms and may include physical therapy, educational support, and medical care for any health problems.&lt;br /&gt;
&lt;br /&gt;
== See also ==&lt;br /&gt;
&lt;br /&gt;
* [[Genetic disorder]]&lt;br /&gt;
* [[Chromosome abnormality]]&lt;br /&gt;
* [[Genetic testing]]&lt;br /&gt;
* [[Karyotype]]&lt;br /&gt;
* [[Microarray analysis]]&lt;br /&gt;
* [[Next-generation sequencing]]&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
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&amp;lt;references /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{{stub}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetic disorders]]&lt;br /&gt;
[[Category:Chromosomal abnormalities]]&lt;br /&gt;
[[Category:Medical conditions]]&lt;br /&gt;
[[Category:Syndromes]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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