Noonan syndrome: genetic and clinical update and treatment options

• Hauptverfasser: Atilano Carcavilla (Verfasst von), Larisa Suárez-Ortega (Verfasst von), Amparo Rodríguez Sánchez (Verfasst von), Isabel Gonzalez-Casado (Verfasst von), Marta Ramón-Krauel (Verfasst von), Jose Ignacio Labarta (Verfasst von), Sofia Quinteiro Gonzalez (Verfasst von), Isolina Riaño Galán (Verfasst von), Juan Pedro López-Siguero (Verfasst von)
• Format: Buch
• Veröffentlicht: Elsevier, 2020-07-01T00:00:00Z.
• Schlagworte: article
• Online-Zugang: Connect to this object online.

Noonan syndrome (NS) is a relatively common genetic condition characterised by short stature, congenital heart defects, and distinctive facial features.NS and other clinically overlapping conditions such as NS with multiple lentigines (formerly called "LEOPARD" syndrome), cardiofaciocutane...