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- W52727301 abstract "Noonan syndrome is a relatively common autosomal dominant genetic disorder which is characterised by typical facial features, congenital heart diseases and small stature. In 50% of the cases the syndrome is caused by a mutation on the PTPN11-gen. The expression of symptoms associated with Noonan syndrome can be very mild in nature and facial features usually become less pronounced with age, which can sometimes make a correct diagnosis more difficult. Despite a wide range of associated symptoms most adults with Noonan syndrome can be self-sustaining, with a good quality of life. It is important that the dentist is well-informed about this syndrome due to the heart diseases and bleeding disorders which can be present with these patients and may influence a dentist's choice of therapy when invasive treatment is indicated." @default.
- W52727301 created "2016-06-24" @default.
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- W52727301 date "2013-12-06" @default.
- W52727301 modified "2023-09-24" @default.
- W52727301 title "Een patiënt met het syndroom van Noonan" @default.
- W52727301 doi "https://doi.org/10.5177/ntvt.2013.12.13165" @default.
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- W52727301 hasPublicationYear "2013" @default.
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