Noonan syndrome (NS) was described by Noonan and Ehmke as a multi-system disorder, which is typically evident at birth. The incidence of this syndrome is estimated to be one per 2500 to one per 1000 and affects both genders. While the clinical manifestations of NS have been well documented, the oral manifestations have not been extensively discussed. The purpose of the present article is to (a) review the oral manifestations of NS reported in the literature, and (b) describe four cases (three females and one male) of NS, who presented with short stature, cardiac problems and various oral findings. Based on these cases, we conclude that many oral anomalies may have possible relationships with NS, which require multidisciplinary treatment pla...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Aims: Noonan syndrome (NS) is a clinically and genetically heterogeneous condition characterized by ...
"nNoonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many...
Noonan Syndrome (NS) is an autosomal dominant condition caused by mutations in multiple genes in the...
Noonan syndrome (NS) is an autosomal dominant inherited disorder. NS can be confirmed genetically by...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
The present report describes a case of Noonan’s syndrome from a dental viewpoint. Noonan syndrome is...
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagn...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Aims: Noonan syndrome (NS) is a clinically and genetically heterogeneous condition characterized by ...
"nNoonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many...
Noonan Syndrome (NS) is an autosomal dominant condition caused by mutations in multiple genes in the...
Noonan syndrome (NS) is an autosomal dominant inherited disorder. NS can be confirmed genetically by...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
The present report describes a case of Noonan’s syndrome from a dental viewpoint. Noonan syndrome is...
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagn...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Oral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination ...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...