Do you know this syndrome?

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...

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Podrobná bibliografie
Hlavní autoři: Kondo, Rogerio Nabor, Martins, Ligia Márcia Mario, Lopes, Vivian Cristina Holanda, Bittar, Rodrigo Antonio, Araújo, Fernanda Mendes
Médium: Artigo
Jazyk:Inglês
Vydáno: Sociedade Brasileira de Dermatologia 2013
Témata:
Syndrome in Question
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3760954/
https://ncbi.nlm.nih.gov/pubmed/24068150
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20131934
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