Add to ORKGOral findings in a case of Noonan syndrome in an 8-year-old Japanese male are reported. Examination of the patient revealed a narrow, higharched palate and an anterior open bite. Cephalometric measurements showed a wide gonial angle, a large mandibular plane angle, a large Y-axis and long facial height. It is suggested that the patient had a skeletal open-bite malocclusion, which included an abnormal swallowing habit
Noonan syndrome (NS) is an autosomal dominant inherited disorder. NS can be confirmed genetically by...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
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 ...
Aims: Noonan syndrome (NS) is a clinically and genetically heterogeneous condition characterized by ...
Noonan Syndrome (NS) is an autosomal dominant condition caused by mutations in multiple genes in the...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Noonan syndrome (NS) was described by Noonan and Ehmke as a multi-system disorder, which is typicall...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
Objective: To evaluate orodental, facial, clinical and molecular characteristics of the patients wit...
The present report describes a case of Noonan’s syndrome from a dental viewpoint. Noonan syndrome is...
"nNoonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many...
To date, only a limited number of publications have studied the specific oral and maxillofacial find...
Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long...
Noonan syndrome (NS) is an autosomal dominant inherited disorder. NS can be confirmed genetically by...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
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 ...
Aims: Noonan syndrome (NS) is a clinically and genetically heterogeneous condition characterized by ...
Noonan Syndrome (NS) is an autosomal dominant condition caused by mutations in multiple genes in the...
Background/Aim: Noonan syndrome (NS) is an autosomal dominant disorder, caused by mutations on genes...
Noonan syndrome (NS) was described by Noonan and Ehmke as a multi-system disorder, which is typicall...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...
Objective: To evaluate orodental, facial, clinical and molecular characteristics of the patients wit...
The present report describes a case of Noonan’s syndrome from a dental viewpoint. Noonan syndrome is...
"nNoonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many...
To date, only a limited number of publications have studied the specific oral and maxillofacial find...
Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long...
Noonan syndrome (NS) is an autosomal dominant inherited disorder. NS can be confirmed genetically by...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome is a developmental disorder characterized by facial dysmorphia, short stature, cardi...