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	<title>Ruvalcaba syndrome - Revision history</title>
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	<updated>2026-04-25T19:18:29Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=Ruvalcaba_syndrome&amp;diff=2374059&amp;oldid=prev</id>
		<title>Deepika vegiraju at 13:46, 19 April 2021</title>
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		<updated>2021-04-19T13:46:19Z</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;Definition&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Ruvalcaba syndrome is an extremely rare malformation syndrome, described in less than 10 patients to date, characterized by [[microcephaly]] with characteristic facies (downslanting [[parpebral fissure]], [[microstomia]], beaked nose, narrow maxilla), very short stature, narrow thoracic cage with pectus carinatum, hypoplastic genitalia and skeletal anomalies (i.e. characteristic [[brachydactyly]] and [[osteochondritis]] of the spine) as well as intellectual and [[developmental delay]].&lt;br /&gt;
&lt;br /&gt;
{{rarediseases}}&lt;br /&gt;
{{stb2}}&lt;/div&gt;</summary>
		<author><name>Deepika vegiraju</name></author>
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