Noonan Syndrome Latest Advances

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery

Published: January 18, 2026

Noonan Syndrome Latest Advances

Find the Latest Research About Noonan Syndrome

An Unexpected Result in a Case of Gonadal Dysgenesis: Noonan Syndrome Caused by RIT1 Mutation.

An Unexpected Result in a Case of Gonadal Dysgenesis: Noonan Syndrome Caused by RIT1 Mutation.

Effects of neighborhood level health and environment quality on academic and executive abilities in youth with Noonan syndrome spectrum disorder.

Effects of neighborhood level health and environment quality on academic and executive abilities in youth with Noonan syndrome spectrum disorder.

Restoring the 14-3-3/CRAF regulatory interaction in Noonan syndrome using molecular glues.

Restoring the 14-3-3/CRAF regulatory interaction in Noonan syndrome using molecular glues.

Preterm Noonan syndrome with generalised venolymphatic malformation.

Preterm Noonan syndrome with generalised venolymphatic malformation.

Irreversible blindness induced by vitamin A deficiency in a child with avoidant/restrictive food intake disorder secondary to Noonan syndrome.

Irreversible blindness induced by vitamin A deficiency in a child with avoidant/restrictive food intake disorder secondary to Noonan syndrome.

Molecular Diagnosis and Phenotypic Variability of Noonan Syndrome: Experience from a Romanian Multicenter Study.

Molecular Diagnosis and Phenotypic Variability of Noonan Syndrome: Experience from a Romanian Multicenter Study.

Blunt Trauma-Induced Chylothorax in Noonan Syndrome: A Rare Clinical Presentation.

Blunt Trauma-Induced Chylothorax in Noonan Syndrome: A Rare Clinical Presentation.

Trametinib Therapy for Hypertrophic Cardiomyopathy and Pulmonary Hypertension in a Child With RAF1-Related Noonan Syndrome (p.Ser257Leu): A Case Report.

Trametinib Therapy for Hypertrophic Cardiomyopathy and Pulmonary Hypertension in a Child With RAF1-Related Noonan Syndrome (p.Ser257Leu): A Case Report.

PTPN11-Related Noonan Syndrome Predisposes to Multifocal Low-Grade CNS Tumors Harboring FGFR1 Variants.

PTPN11-Related Noonan Syndrome Predisposes to Multifocal Low-Grade CNS Tumors Harboring FGFR1 Variants.

From case reports to a cohort: illuminating the spectrum of pulmonary hypertension in Noonan syndrome.

From case reports to a cohort: illuminating the spectrum of pulmonary hypertension in Noonan syndrome.

PTPN11-related Noonan syndrome predisposes to multifocal low-grade CNS tumors harboring FGFR1 variants.

PTPN11-related Noonan syndrome predisposes to multifocal low-grade CNS tumors harboring FGFR1 variants.

Largely preserved vestibular function despite severe-to-profound hearing loss in Noonan syndrome spectrum disorders.

Largely preserved vestibular function despite severe-to-profound hearing loss in Noonan syndrome spectrum disorders.