Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
BMJ Case Rep ; 20152015 Feb 25.
Article in English | MEDLINE | ID: mdl-25716036

ABSTRACT

Noonan syndrome is an autosomal dominant disorder with genetically heterogeneous inheritance. The incidence of cardiac abnormalities is higher in patients with Noonan syndrome and approximately 80% patients with Noonan syndrome are reported to have cardiac abnormalities during their lifetimes. However, polyvalvular disease in Noonan syndrome is rare. In this case-report, we describe a case of a young man whose features were strongly suggestive of Noonan syndrome and who was diagnosed with prolapse of all four cardiac valves after 22 years of uneventful survival.


Subject(s)
Abnormalities, Multiple/genetics , Heart Defects, Congenital/genetics , Heart Valve Prolapse/genetics , Noonan Syndrome/genetics , Abnormalities, Multiple/diagnosis , Adult , Diagnosis, Differential , Face/abnormalities , Heart Defects, Congenital/diagnosis , Heart Valve Prolapse/diagnosis , Humans , Intellectual Disability/genetics , Male , Noonan Syndrome/diagnosis
SELECTION OF CITATIONS
SEARCH DETAIL
...