Limits...
Do you know this syndrome? Noonan syndrome.

Kondo RN, Martins LM, Lopes VC, Bittar RA, Araújo FM - An Bras Dermatol (2013 Jul-Aug)

Bottom Line: Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children presenting with syndromic facies similar to Turner's syndrome phenotype.This syndrome is characterized by facial dysmorphism, congenital heart defects, short stature and also a wide phenotypic variation.This article discusses the case of a 10 year-old patient with Noonan syndrome that presented typical facies, cardiac defects (pulmonary dilatation and mitral regurgitation), dental malocclusion, micrognatism, short stature and a certain degree of learning disability.

View Article: PubMed Central - PubMed

Affiliation: Hospital Universitário Regional do Norte do Paraná, State University of Londrina, Londrina(PR),Brazil.

ABSTRACT
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children presenting with syndromic facies similar to Turner's syndrome phenotype. This syndrome is characterized by facial dysmorphism, congenital heart defects, short stature and also a wide phenotypic variation. This article discusses the case of a 10 year-old patient with Noonan syndrome that presented typical facies, cardiac defects (pulmonary dilatation and mitral regurgitation), dental malocclusion, micrognatism, short stature and a certain degree of learning disability.

Show MeSH

Related in: MedlinePlus

Hypertelorism, downward slanting palpebral fissures, micrognathia, ptosis and short neck
© Copyright Policy - open-access
Related In: Results  -  Collection

License
getmorefigures.php?uid=PMC3760954&req=5

f02: Hypertelorism, downward slanting palpebral fissures, micrognathia, ptosis and short neck

Mentions: Physical examination showed signs of hypertelorism, down-slanting palpebral fissures, low set posteriorly rotated ears, palpebral ptosis, short neck, micrognathism and short stature (Figures 1 and 2). The mother reported some degree of learning disability and the need for special educational support in school.


Do you know this syndrome? Noonan syndrome.

Kondo RN, Martins LM, Lopes VC, Bittar RA, Araújo FM - An Bras Dermatol (2013 Jul-Aug)

Hypertelorism, downward slanting palpebral fissures, micrognathia, ptosis and short neck
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3760954&req=5

f02: Hypertelorism, downward slanting palpebral fissures, micrognathia, ptosis and short neck
Mentions: Physical examination showed signs of hypertelorism, down-slanting palpebral fissures, low set posteriorly rotated ears, palpebral ptosis, short neck, micrognathism and short stature (Figures 1 and 2). The mother reported some degree of learning disability and the need for special educational support in school.

Bottom Line: Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children presenting with syndromic facies similar to Turner's syndrome phenotype.This syndrome is characterized by facial dysmorphism, congenital heart defects, short stature and also a wide phenotypic variation.This article discusses the case of a 10 year-old patient with Noonan syndrome that presented typical facies, cardiac defects (pulmonary dilatation and mitral regurgitation), dental malocclusion, micrognatism, short stature and a certain degree of learning disability.

View Article: PubMed Central - PubMed

Affiliation: Hospital Universitário Regional do Norte do Paraná, State University of Londrina, Londrina(PR),Brazil.

ABSTRACT
Noonan Syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children presenting with syndromic facies similar to Turner's syndrome phenotype. This syndrome is characterized by facial dysmorphism, congenital heart defects, short stature and also a wide phenotypic variation. This article discusses the case of a 10 year-old patient with Noonan syndrome that presented typical facies, cardiac defects (pulmonary dilatation and mitral regurgitation), dental malocclusion, micrognatism, short stature and a certain degree of learning disability.

Show MeSH
Related in: MedlinePlus