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Http://dbpedia.org/resource/DeSanto-Shinawi syndrome
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http://dbpedia.org/resource/DeSanto-Shinawi_syndrome
http://dbpedia.org/ontology/abstract DeSanto-Shinawi (DESSH) syndrome is a rareDeSanto-Shinawi (DESSH) syndrome is a rare genetic disorder caused by genetic variations (mutations) in a gene called WW Domain-Containing Adaptor with Coiled-coil Region (the WAC gene). The condition was first described in 2015 in six individuals. The prevalence of DESSH syndrome is unknown at this time, but 25 individuals have been so far described in the medical literature. However, many other individuals with this condition are being studied and characterized. With the increasing utilization of exome and whole genome sequencing, it is anticipated that many more individuals to be identified. The condition is characterized by a variable degree of developmental delay and intellectual disability, decreased muscle tone (hypotonia), behavioral abnormalities, some facial differences, gastrointestinal and eye abnormalities.s, gastrointestinal and eye abnormalities.
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http://dbpedia.org/property/management Physical, occupational and speech therapy
http://dbpedia.org/property/name DeSanto-Shinawi syndrome
http://dbpedia.org/property/onset http://dbpedia.org/resource/Infancy +
http://dbpedia.org/property/specialty http://dbpedia.org/resource/Neurology + , http://dbpedia.org/resource/Medical_genetics +
http://dbpedia.org/property/symptoms Specific developmental disorder, intellectual disability, hypotonia, behavioral abnormalities, facial differences, gastrointestinal and eye abnormalities
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rdfs:comment DeSanto-Shinawi (DESSH) syndrome is a rareDeSanto-Shinawi (DESSH) syndrome is a rare genetic disorder caused by genetic variations (mutations) in a gene called WW Domain-Containing Adaptor with Coiled-coil Region (the WAC gene). The condition was first described in 2015 in six individuals. The prevalence of DESSH syndrome is unknown at this time, but 25 individuals have been so far described in the medical literature. However, many other individuals with this condition are being studied and characterized. With the increasing utilization of exome and whole genome sequencing, it is anticipated that many more individuals to be identified.at many more individuals to be identified.
rdfs:label DeSanto-Shinawi syndrome
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