MOWAT-WILSON SYNDROME FOUNDATION
This is the official page for the Mowat-Wilson Syndrome Foundation. The mission of The Mowat-Wilson Foundation is to enhance the lives of people affected by Mowat-Wilson Syndrome by providing family support, raising awareness, and supporting research and education. Mowat-Wilson Syndrome is a recently discovered syndrome (defined in 1998) and much is still being learned about the physical, behavioral and developmental issues associated with this rare genetic disorder. Major signs include: distinctive facial features, intellectual disability, delayed development, intestinal disorders, seizures, congenital heart disease, agenesis of the corpus callosum, male genital abnormalities (hypospadias), and major expressive language difficulty.
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Mowat-Wilson Syndrome Foundation Research. Support. Hope. LEARN MORE Our mission is to enhance the lives of people affected by MowatWilson Syndrome Family Support Raise Awareness Research A community of support for rare special children and their families DONATE TODAY.
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What innovative strategies can the Mowat-Wilson Syndrome Foundation implement to increase awareness and support for families affected by Mowat-Wilson Syndrome?
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Brooklyn Simmons
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How can we leverage social media more effectively to connect families and share resources within the Mowat-Wilson Syndrome community?
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Together, we can make a real impact in communities around the world. Help us bring hope and support.
So grateful for all the work the Mowat-Wilson Syndrome Foundation does! 🌟 Together, we can raise awareness and support families affected by this rare disorder. 💙 #MWSF
Brooklyn Simmons
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Excited for the upcoming research webinar! It's amazing to see how much progress is being made in understanding and supporting individuals with Mowat-Wilson Syndrome. Let's keep the hope alive! 🙌 #MWSF2025
Brooklyn Simmons
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