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Bookmark or Share- Home - marshallsmith.orgMarshall-Smith Syndrome: Rare but strong together. The Marshall-Smith syndrome (MSS) is a very infrequently described syndrome. The syndrome has been described for the first time in 1971. Since then, about 50 children and adults with the syndrome are known in the medical literature worldwide.
- Marshall-Smith syndrome - About the Disease - Genetic and Rare Diseases ...Marshall-Smith syndrome (MRSHSS) is a genetic disorder in which individuals typically have advanced bone age, difficulties gaining weight (failure to thrive), unique facial features, and intellectual disability. Other signs and symptoms of this condition may include eye abnormalities, breathing difficulties, and neurological issues.
- Marshall Smith Syndrome - Symptoms, Causes, Treatment | NORDMarshall-Smith Syndrome is a rare disorder that has only been documented in about 50 individuals worldwide. It appears to affect males and females equally. Symptoms are typically present at birth, such as the previously escribed characteristic facial features.
- Nonprofit Organization Providing Marshall-Smith Syndrome InformationMarshall-Smith Syndrome Organization of the USA. info@mss-usa.org. Learn about Marshall-Smith Syndrome and find valuable information through our nonprofit organization dedicated to raising awareness and supporting individuals with this rare condition.
- The Marshall-Smith Syndrome Association of the United StatesMarshall-Smith syndrome (MSS) is an ultra-rare, genetic disorder that causes multiple congenital anomalies. MSS was first described in 1971 by physicians R.E. Marshall, C.B. Graham, C.R. Scott, and D.W. Smith. Since then, fewer than 100 cases have been described in worldwide medical literature.
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