DBMCI - MDS Experts : the NEET MDS Experts - NOONAN SYNDROME • Also k/as Noonan-neurofibromatosis Syndrome. • It is caused by mutation in neurofibromin gene. Clinical Features: • Broad forehead, Drooping
Pin by nonas arc on Noonan Syndrome | Noonan syndrome, Congenital heart defect, Heart defect
Noonan Syndrome
The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome | European Journal of Human Genetics
Noonan Syndrome - Causes, Symptoms, Diagnosis and Treatment
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome | Journal of Medical Genetics
Noonan syndrome‐like disorder with loose anagen hair: A second case with neuroblastoma - Garavelli - 2015 - American Journal of Medical Genetics Part A - Wiley Online Library
Dental and maxillofacial features of Noonan Syndrome: Case series of ten patients - ScienceDirect