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Pregnancy Timeline by SemestersFemale Reproductive SystemFertilizationThe Appearance of SomitesFirst TrimesterSecond TrimesterThird TrimesterFetal liver is producing blood cellsHead may position into pelvisBrain convolutions beginFull TermWhite fat begins to be madeWhite fat begins to be madeHead may position into pelvisImmune system beginningImmune system beginningPeriod of rapid brain growthBrain convolutions beginLungs begin to produce surfactantSensory brain waves begin to activateSensory brain waves begin to activateInner Ear Bones HardenBone marrow starts making blood cellsBone marrow starts making blood cellsBrown fat surrounds lymphatic systemFetal sexual organs visibleFinger and toe prints appearFinger and toe prints appearHeartbeat can be detectedHeartbeat can be detectedBasic Brain Structure in PlaceThe Appearance of SomitesFirst Detectable Brain WavesA Four Chambered HeartBeginning Cerebral HemispheresEnd of Embryonic PeriodEnd of Embryonic PeriodFirst Thin Layer of Skin AppearsThird TrimesterDevelopmental Timeline
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April 10, 2012--------News Archive Return to: News Alerts

As more DNA sequence variations are discovered, medical science
may find new ways to intervene in the disabling disorder.

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Genetic Mutations at Conception Linked to Many Cases of Autism

About 15 percent of autism cases in families with a single autistic child are associated with spontaneous mutations that occur in sex cells

The findings are the result of DNA sequencing of every gene in 238 families, each with only one autistic child — the most sophisticated analysis yet of the genetic links to autism. The study identified hundreds of such de novo or spontaneous sequence variations, and as more are discovered, medical science may find new ways to intervene in the disabling disorder, the authors say.

Yale University researchers reported their findings in the April 4 issue of the journal Nature.

The Yale team, in cooperation with researchers at Carnegie Mellon University, the University of Pittsburgh and UCLA, also linked variations in three specific genes to a markedly increased risk for autism.

"Prior to the advent of new DNA sequencing technology, we were largely wandering in the dark searching for autism genes," said Matthew State, senior author, the Donald J. Cohen Professor of Child Psychiatry, psychiatry and genetics, and co-director of the Yale Program on Neurogenetics. "Now we are getting a clear view of the genetic landscape and finally have the tools in hand to find a large proportion of the many genes contributing to autism."

The genetic underpinnings of autism have been the subject of intensive research. Twin studies reveal a strong genetic component to autism but a substantial number of cases occur in families with no known history. Recent research has focused on genetic mutations that may arise at conception.

The new Yale study also showed that these de novo mutations were more frequent in children born to older fathers, offering at least a partial explanation for the increased risk for autism in children of older parents.

The researchers expect that, with additional DNA studies, the percentage of autism cases linked to these de novo mutations will increase—and with it the ability to detect and treat the disorder.

"With every new gene we discover, we learn more about potential treatments for patients with autism," said Stephan Sanders, pediatrician, a postdoctoral fellow in State's lab and lead author of the Nature paper.

The study was funded by the Simons Foundation.

Other Yale researchers include Michael T. Murtha, Abha R. Gupta, John D. Murdoch, Melanie J. Raubeson, A. Jeremy Willsey, A. Gulhan Ercan-Sencicek, Nicholas M. DiLullo, Michael F. Walker, Gordon T. Ober, Youeun Song, Paul El-Fishawy, Ryan C. Murtha, Murim Choi, John D. Overton, Robert D. Bjornson, Nicholas J. Carriero, Kyle A. Meyer, Kaya Bilguvar, Shrikant M. Mane, Nenad Šestan, Richard P. Lifton, and Murat Günel.

Original article: http://www.eurekalert.org/pub_releases/2012-04/yu-gma040212.php