The Prevalence of Clinical Features in Patients with Aarskog–Scott Syndrome and Assessment of Genotype-Phenotype Correlation: A Systematic Review

Aarskog–Scott syndrome is a genetically and clinically heterogeneous rare condition caused by a pathogenic variant in the FGD1 gene. A systematic review was carried out to analyse the prevalence of clinical manifestations found in patients, as well as to evaluate the genotype-phenotype correlation....

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Detalles Bibliográficos
Autores principales: Zanetti Drumond, Victor, Sousa Salgado, Lucas, Sousa Salgado, Camila, Oliveira, Vitor Augusto de Lima, de Assis, Eliene Magda, Campos Ribeiro, Michel, Furtado Valadão, Analina, Orrico, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953535/
https://www.ncbi.nlm.nih.gov/pubmed/33762894
http://dx.doi.org/10.1155/2021/6652957

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953535/
https://www.ncbi.nlm.nih.gov/pubmed/33762894
http://dx.doi.org/10.1155/2021/6652957

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