A Case of Sotos Syndrome in a Preterm Infant with Severe Bronchopulmonary Dysplasia and Congenital Heart Disease

Sotos syndrome is an autosomal dominant genetic disorder caused by mutations in the NSD1 gene. In this study, we report a case of Sotos syndrome in a preterm infant. The main clinical manifestations were severe bronchopulmonary dysplasia, congenital heart disease, difficulty feeding, and characteris...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Dan-Fang, Tong, Xiao-Mei, Liu, Yun-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378172/
https://www.ncbi.nlm.nih.gov/pubmed/37508608
http://dx.doi.org/10.3390/children10071111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378172/
https://www.ncbi.nlm.nih.gov/pubmed/37508608
http://dx.doi.org/10.3390/children10071111

Ejemplares similares