Noonan Syndrome Latest Advances

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

Journal: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne

Published: March 02, 2026

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

Journal: Cureus

Published: February 25, 2026

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

Journal: Research square

Published: February 06, 2026

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

Journal: Journal of neuro-oncology

Published: January 21, 2026

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

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

Development and Treatment of Severe Lordoscoliosis in a Patient With Noonan Syndrome With Multiple Lentigines (NSML): A Case Report.

Journal: Cureus

Published: January 11, 2026

Ventricular arrhythmia and Noonan syndrome with leucine zipperlike transcription regulator 1 mutations: expanding the phenotype with a case report and review of the literature.

Journal: Cardiology in the young

Published: January 02, 2026

Complex Genetic Architecture in RASopathies: Constitutional PTPN11 and Mosaic RIT1 Pathogenic Variants Underlying Severe Noonan Syndrome With Adult-Onset Acute Myeloid Leukemia.

Journal: American journal of medical genetics. Part A

Published: December 18, 2025

Long-term effectiveness and safety of daily growth hormone therapy in Japanese children with Noonan syndrome: a post-marketing surveillance study.

Journal: Endocrine journal

Published: November 24, 2025

Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigree.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences

Published: November 24, 2025

Current opinions on Noonan syndrome and RASopathies.

Journal: Current opinion in pediatrics

Published: November 13, 2025

Heterogeneity of Orodental Features in a Family with Noonan Syndrome.

Journal: International journal of molecular sciences

Published: November 06, 2025

Noonan Syndrome Latest Advances

Find the Latest Research About Noonan Syndrome

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.

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

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

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.

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.

Development and Treatment of Severe Lordoscoliosis in a Patient With Noonan Syndrome With Multiple Lentigines (NSML): A Case Report.

Development and Treatment of Severe Lordoscoliosis in a Patient With Noonan Syndrome With Multiple Lentigines (NSML): A Case Report.

Ventricular arrhythmia and Noonan syndrome with leucine zipperlike transcription regulator 1 mutations: expanding the phenotype with a case report and review of the literature.

Ventricular arrhythmia and Noonan syndrome with leucine zipperlike transcription regulator 1 mutations: expanding the phenotype with a case report and review of the literature.

Complex Genetic Architecture in RASopathies: Constitutional PTPN11 and Mosaic RIT1 Pathogenic Variants Underlying Severe Noonan Syndrome With Adult-Onset Acute Myeloid Leukemia.

Complex Genetic Architecture in RASopathies: Constitutional PTPN11 and Mosaic RIT1 Pathogenic Variants Underlying Severe Noonan Syndrome With Adult-Onset Acute Myeloid Leukemia.

Long-term effectiveness and safety of daily growth hormone therapy in Japanese children with Noonan syndrome: a post-marketing surveillance study.

Long-term effectiveness and safety of daily growth hormone therapy in Japanese children with Noonan syndrome: a post-marketing surveillance study.

Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigree.

Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigree.

Current opinions on Noonan syndrome and RASopathies.

Current opinions on Noonan syndrome and RASopathies.

Heterogeneity of Orodental Features in a Family with Noonan Syndrome.

Heterogeneity of Orodental Features in a Family with Noonan Syndrome.