Add to ORKGThe term Noonan syndrome has been applied to phenotypic male and female who have certain anomalies that occur also in female with Turner’s syndrome. These patients have normal karyotype. The disorder is very rare. The most common abnormality are short stature, webbing of the neck, Pectus Carinatum or Pectus excavatum, congenital heart disease. This particular case is a 8-year-old girl-patient who referred to pediatric clinic with short stature. Another abnormality in these patients is abnormal facies (Hypertelorism, hypogonadism, piqure chest and webbing of the neck). The patient had moderate mental retardation. Chromosomal analysis revealed 46xx cytogenetic distinguished Noonan syndrome
Background Turner syndrome (TS) and Noonan syndrome (NS) share some phenotypical similarities: short...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
A case of Noonan syndrome in an Indonesian baby boy is reported. The diagnosis was based on history,...
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagn...
Five patients with cardiovascular anomalies and Noonan's syndrome are described. In each instance, p...
Five patients with cardiovascular anomalies and Noonan's syndrome are described. In each instance, p...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
BACKGROUND Noonan syndrome (NS) is an autosomal dominant disorder characterised by genotypic and phe...
Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long...
Noonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many affect...
Noonan syndrome is a common genetic disorder characterized by facial anomalies, congenital heart de...
*Author for Correspondence Noonan syndrome [NS] is an autosomal dominant inherited condition that ca...
Background Turner syndrome (TS) and Noonan syndrome (NS) share some phenotypical similarities: short...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
A case of Noonan syndrome in an Indonesian baby boy is reported. The diagnosis was based on history,...
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagn...
Five patients with cardiovascular anomalies and Noonan's syndrome are described. In each instance, p...
Five patients with cardiovascular anomalies and Noonan's syndrome are described. In each instance, p...
Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphology and congenital ...
Noonan Syndrome is a rare, autosomal dominant disorder characterized by short stature, facial abnorm...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Contains fulltext : 53073.pdf ( ) (Open Access)Noonan Syndrome (NS) is characteris...
BACKGROUND Noonan syndrome (NS) is an autosomal dominant disorder characterised by genotypic and phe...
Background Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long...
Noonan syndrome is an autosomal dominant disorder that is typically evident at birth. In many affect...
Noonan syndrome is a common genetic disorder characterized by facial anomalies, congenital heart de...
*Author for Correspondence Noonan syndrome [NS] is an autosomal dominant inherited condition that ca...
Background Turner syndrome (TS) and Noonan syndrome (NS) share some phenotypical similarities: short...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
A case of Noonan syndrome in an Indonesian baby boy is reported. The diagnosis was based on history,...