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First Report of New Oral Findings in a Case with Noonan Syndrome
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نویسنده
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Sahebjamee M ,Ameri NG ,Farhud DD
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منبع
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iranian journal of public health - 2008 - دوره : 37 - شماره : 4 - صفحه:131 -137
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چکیده
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Noonan syndrome is an autosomal dominant disorder that is typically evident at birth. in many affected individuals, this syndrome is associated with cardiac defects and a distinctive facial appearance. the high frequency of cardiac disorder,ophthalmic, growth and orthopedic signs, associated with noonan syndrome emphasizes the need for early diagnosis. thisreport aimed to present a 19 year old iranian girl suffering from noonan syndrome. in this case in addition to typical signsand symptoms reported for noonan syndrome earlier, there are three other significant signs which have not been reportedyet in any other cases. so they are supposed to be related to noonan syndrome.
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کلیدواژه
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Noonan syndrome ,Taurodontism ,Prominent rugae ,Missing canine ,Iran
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آدرس
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tehran university of medical sciences tums, Faculty of Dentistry, Dept of Oral Medicine, ایران, tehran university of medical sciences tums, Faculty of Dentistry, Dept of Oral Medicine, ایران, Genetic Clinic, ایران
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پست الکترونیکی
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sahebjam@sina.tums.ac.ir
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Authors
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