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--- content:aicardi_syndrome [2020/02/13 13:28] – [Genetics] icna
+++ content:aicardi_syndrome [2020/02/23 00:47] – icna
@@ Line 36: / Line 36: @@
   * The presence of two classical features in addition to at least two major or supporting features is strongly suggestive of a diagnosis of Aicardi syndrome
 ==== Genetics ====
-Nearly all reported cases of Aicardi syndrome are sporadic and in females. The disorder is believed to result from new gene mutations. Aicardi syndrome is classified as an X-linked dominant condition[{{ :content:xlinkdominant.jpeg?300|Credit:U.S National Library of Medicine}}. In 2015 mutation in gene [[https://www.genecards.org/cgi-bin/carddisp.pl?gene=TEAD1|TEAD1]] was found to be associated with Aicardi syndrome[(:cite:>{{pubmed>long:26091538}})]. This was the first genetic mutation associated with Aicardi syndrome to be reported. This study also found that TEAD1 mutations may be present in males.
+  * Nearly all reported cases of Aicardi syndrome are sporadic and in females and believed to result from new gene mutations
+  * Aicardi syndrome is classified as an X-linked dominant condition[{{ :content:xlinkdominant.jpeg?300|Credit:U.S National Library of Medicine}}.
+  * mutation in gene [[https://www.genecards.org/cgi-bin/carddisp.pl?gene=TEAD1|TEAD1]] was the first genetic mutation reported to be associated with Aicardi syndrome[(:cite:>{{pubmed>long:26091538}})]. TEAD1 mutations has also been shown to be present in males[(:cite:>{{pubmed>long:26091538}})].
 === Neuroimaging ===