Anterior Uveitis and Coats Disease in a 16-Year-Old Girl with Noonan Syndrome—A Case Report

Background: Noonan syndrome (NS) represents a fairly common genetic disorder with a highly variable phenotype. Its features include inherited heart defects, characteristic facial features, short stature, and mild retardation of motor skills. Case presentation: A 16-year-old Caucasian girl with NS re...

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Detalles Bibliográficos
Autores principales: Świerczyńska, Marta, Tronina, Agnieszka, Lorenc, Anna, Filipek, Erita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605920/
https://www.ncbi.nlm.nih.gov/pubmed/37892306
http://dx.doi.org/10.3390/children10101643

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605920/
https://www.ncbi.nlm.nih.gov/pubmed/37892306
http://dx.doi.org/10.3390/children10101643

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