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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Chromosome_9q_duplication</id>
	<title>Chromosome 9q duplication - Revision history</title>
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	<updated>2026-04-27T15:07:35Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=Chromosome_9q_duplication&amp;diff=2380763&amp;oldid=prev</id>
		<title>Deepika vegiraju at 12:06, 5 June 2021</title>
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		<updated>2021-06-05T12:06:31Z</updated>

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&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== &amp;#039;&amp;#039;&amp;#039;Alternate names&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Duplication 9q; Trisomy 9q; 9q duplication; 9q trisomy; Partial trisomy 9q &lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Definition&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Chromosome 9q duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the long arm (q) of chromosome 9.&lt;br /&gt;
[[File:Human chromosome 9 ideogram.svg|thumb]]&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Cause&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
This condition occurs when there is an &amp;#039;&amp;#039;&amp;#039;extra copy of genetic material on the long arm (q) of chromosome 9&amp;#039;&amp;#039;&amp;#039;.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Inheritance&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Chromosome testing of both parents can provide more information on whether or not the duplication was inherited.&lt;br /&gt;
 In most cases, &amp;#039;&amp;#039;&amp;#039;parents do not have any chromosomal anomaly&amp;#039;&amp;#039;&amp;#039;. &lt;br /&gt;
However, sometimes one parent is found to have a [[balanced translocation]], where a piece of a chromosome has broken off and attached to another one with no gain or loss of genetic material. &lt;br /&gt;
* The balanced translocation normally does not cause any signs or symptoms, but it increases the risk for having an affected child with a chromosomal anomaly like a [[duplication]].&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Signs and symptoms&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
* The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. &lt;br /&gt;
* Features that often occur in people with chromosome 9q duplication include [[developmental delay]], [[intellectual disability]], behavioral problems and distinctive facial features.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Diagnosis&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Chromosome disorders may be suspected in people who have developmental delays, intellectual disabilities and/or physical abnormalities. &lt;br /&gt;
&lt;br /&gt;
Several types of genetic tests can identify chromosome disorders: &lt;br /&gt;
* [[Karyotyping]]&lt;br /&gt;
* [[Microarray]] (also called array CGH)&lt;br /&gt;
* [[Fluorescence in situ hybridization (FISH)]]&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Treatment&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Treatment is based on the signs and symptoms present in each person.&lt;br /&gt;
&lt;br /&gt;
{{rarediseases}}&lt;br /&gt;
{{stb}}&lt;/div&gt;</summary>
		<author><name>Deepika vegiraju</name></author>
	</entry>
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