Noonan Syndrome
Dec. 25, 2024
Noonan Syndrome | AAFP DBMCI MDS : Formerly MDS Experts - Noonan Syndrome • Also k/as Noonan-neurofibromatosis Syndrome. • It is caused by mutation in neurofibromin gene. Clinical features: • Broad forehead, Drooping eyelid (ptosis). • PDF] Patients With Noonan Syndrome Phenotype: Spectrum Of Clinical FeaturesAnd Congenital Heart Defect | Semantic Scholar Noonan Syndrome