Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long arm of chromosome 72. Case report The authors examined a caucasic girl of eight years with Noonan syndrome. The patient had systemic problems, such as: otitis, heart trouble, language disturbances and asymmetry of the lower limbs. Light mental delay was also found. She had the bad habit of sucking the lower lip. The treatment plan was extraction of some teeth, sealing of first molars and orthodontic treatment with functional appliance
Noonan syndrome is a clinically and genetically heterogeneous condition characterized by distinctive...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
Noonan syndrome (NS) was described by Noonan and Ehmke as a multi-system disorder, which is typicall...
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...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Noonan syndrome is a congenital developmental disorder characterized by short stature, facial dysmor...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagn...
The term Noonan syndrome has been applied to phenotypic male and female who have certain anomalies t...
Aims: Noonan syndrome (NS) is a clinically and genetically heterogeneous condition characterized by ...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
Noonan Syndrome (NS) is an autosomal dominant condition caused by mutations in multiple genes in the...
To date, only a limited number of publications have studied the specific oral and maxillofacial find...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a clinically and genetically heterogeneous condition characterized by distinctive...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
Noonan syndrome (NS) was described by Noonan and Ehmke as a multi-system disorder, which is typicall...
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...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Noonan syndrome is a congenital developmental disorder characterized by short stature, facial dysmor...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagn...
The term Noonan syndrome has been applied to phenotypic male and female who have certain anomalies t...
Aims: Noonan syndrome (NS) is a clinically and genetically heterogeneous condition characterized by ...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
Noonan Syndrome (NS) is an autosomal dominant condition caused by mutations in multiple genes in the...
To date, only a limited number of publications have studied the specific oral and maxillofacial find...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a clinically and genetically heterogeneous condition characterized by distinctive...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
Noonan syndrome (NS) was described by Noonan and Ehmke as a multi-system disorder, which is typicall...