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	<title>VACTERL hydrocephaly - Revision history</title>
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	<updated>2026-04-22T10:30:08Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.com/index.php?title=VACTERL_hydrocephaly&amp;diff=6195394&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2025-02-04T06:55:40Z</updated>

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		<author><name>Prab</name></author>
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	<entry>
		<id>https://wikimd.com/index.php?title=VACTERL_hydrocephaly&amp;diff=5471150&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-03-30T20:15:09Z</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;VACTERL-Hydrocephaly&amp;#039;&amp;#039;&amp;#039; is a rare disorder that combines features of [[VACTERL association]] with [[hydrocephaly]], a condition characterized by an abnormal accumulation of [[cerebrospinal fluid]] (CSF) in the [[brain]]. VACTERL association is a non-random association of birth defects that affects multiple parts of the body. The acronym VACTERL stands for vertebral defects (V), [[anal atresia]] (A), [[cardiac defects]] (C), [[tracheoesophageal fistula]] (TE) with [[esophageal atresia]], [[renal anomalies]] (R), and limb abnormalities (L). When hydrocephaly is also present, the condition is referred to as VACTERL-H.&lt;br /&gt;
&lt;br /&gt;
==Symptoms and Diagnosis==&lt;br /&gt;
The symptoms of VACTERL-Hydrocephaly vary widely among individuals, depending on the combination and severity of defects. Common symptoms include difficulties with feeding and breathing, heart defects, limb abnormalities, and neurological issues due to hydrocephaly. Diagnosis is typically made based on the physical presence of multiple defects associated with the VACTERL association, along with imaging studies such as [[MRI]] or [[CT scan]] that confirm the presence of hydrocephaly.&lt;br /&gt;
&lt;br /&gt;
==Causes==&lt;br /&gt;
The exact cause of VACTERL-Hydrocephaly is unknown, but it is believed to involve genetic and environmental factors. No specific genetic mutation has been consistently associated with the condition, suggesting a multifactorial inheritance pattern. Environmental factors that may increase the risk include maternal diabetes, obesity, and exposure to certain medications or toxins during pregnancy.&lt;br /&gt;
&lt;br /&gt;
==Treatment==&lt;br /&gt;
Treatment for VACTERL-Hydrocephaly is multidisciplinary and focuses on managing each of the individual defects. Surgical interventions may be necessary for anomalies such as anal atresia, cardiac defects, tracheoesophageal fistula, and hydrocephaly. Ongoing care from specialists in [[pediatrics]], [[cardiology]], [[neurology]], and other fields is often required to address the complex needs of these patients.&lt;br /&gt;
&lt;br /&gt;
==Prognosis==&lt;br /&gt;
The prognosis for individuals with VACTERL-Hydrocephaly varies widely and depends on the number and severity of the birth defects. Early diagnosis and intervention can improve the quality of life and outcomes for many affected individuals.&lt;br /&gt;
&lt;br /&gt;
[[Category:Congenital disorders]]&lt;br /&gt;
[[Category:Neurological disorders]]&lt;br /&gt;
[[Category:Rare diseases]]&lt;br /&gt;
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		<author><name>Prab</name></author>
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