NF2 related schwannomatosis affects everyone differently. It’s a genetic condition that causes tumours to grow on nerves in the brain, inner ear, spinal cord, or peripheral nerves — and it can be truly life changing. Learn more at curenf2.org. #endNF2

Neurofibromatosis type 1 is fully penetrant, so essentially everyone who inherits the mutation develops features of it. But a parent can have skin spots and an ordinary life while their child carries the identical mutation and needs surgery. (3/8)

Delayed diagnosis of neurofibromatosis type I with an index presentation of haemothorax

Managing skin-related adverse events during mirdametinib treatment for NF1-PNs: expert guidance from the ReNeu trial

Early onset scoliosis: A comprehensive review of aetiology, diagnosis and classification

Comparative quantitative analysis of choroidal abnormalities in patients with type 1 neurofibromatosis using multimodal retinal imaging

Bibliometric mapping of the 100 most-cited publications on optic nerve and optic pathway glioma: A cross-sectional bibliometric analysis

Response of Vestibular Schwannomas in NF2-Related Schwannomatosis (NF2-SWN) to Losartan: A Case Series

Inflammatory rhabdomyoblastic tumor: Clinicopathologic and genomic features, association with neurofibromatosis type 1, and progression to rhabdomyosarcoma

Diffuse Eruptive Spitz Nevus With Somatic TPM3::ALK Fusion Confirmed Across Anatomically Distinct Lesions

A Study of Mirdametinib in Infants and Toddlers With Neurofibromatosis Type 1 Associated Plexiform Neurofibromas [NOT_YET_RECRUITING]

Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial) [ACTIVE_NOT_RECRUITING]

Development and Validation of Patient Reported Outcome (PRO) Measures for Individuals With Neurofibromatosis 1 (NF1) and Plexiform Neurofibromas (pNFs) [RECRUITING]

Study of Cabozantinib With Selumetinib for Plexiform Neurofibromas [RECRUITING]

Natural History Study of Patients With Neurofibromatosis Type 2 [RECRUITING]

Clinical, Genetic, and Epidemiologic Study of Children and Adults With RASopathies [RECRUITING]

Targeted Therapy Directed by Genetic Testing in Treating Patients With Locally Advanced or Advanced Solid Tumors, The ComboMATCH Screening Trial [RECRUITING]

Natural History Study of Patients With Neurofibromatosis Type I [ACTIVE_NOT_RECRUITING]

AZD6244 Hydrogen Sulfate for Children With Nervous System Tumors [ACTIVE_NOT_RECRUITING]

Empowering Health: A Focus on Breast Cancer Awareness for Women with NF1 - Neurofibromatosis Network

Carrie Wylie: Championing Hope and Community with NF STRONG Memphis - Neurofibromatosis Network

Pervasive Somatic Mutations in NF1 Drive Cell Type and Spatially Specific Clonal Selection in Neurofibromatosis

Something exciting is coming in 2027! There is no better time to support our charity and our mission! Fix the Gene Change lives! We are putting the FUN into fundraising with an opportunity for you to join us in raising funds where-ever you are in the country.

Standalone NF1: guiding the transition from paediatric to adult care

A 2026 meta-analysis of 50 studies estimated that about 1 in 3 people with neurofibromatosis type 1 (NF1) have ADHD (33%), and that roughly 1 in 10 have autism (11%), seizures (11%), depression (13%), or anxiety (12%).1 https://mentalhealthdaily.com/?p=11702

Pervasive Somatic Mutations in NF1 Drive Cell Type and Spatially Specific Clonal Selection in Neurofibromatosis https://www.biorxiv.org/content/10.64898/2026.09.29.755447v1

Pervasive Somatic Mutations in NF1 Drive Cell Type and Spatially Specific Clonal Selection in Neurofibromatosis https://www.biorxiv.org/content/10.64898/2026.09.29.755447v1

Pervasive Somatic Mutations in NF1 Drive Cell Type and Spatially Specific Clonal Selection in Neurofibromatosis #SingleCell 🧪🧬🖥️ https://www.biorxiv.org/content/10.64898/2026.09.29.755447v1

Inflammatory Rhabdomyoblastic Tumor: Clinicopathologic and Genomic features, Association with Neurofibromatosis Type 1, and Progression to Rhabdomyosarcoma www.sciencedirect.com/science/arti... #hvhebron #ap #onco [Text complet]

When Research Meets Lived Experience: A Young Person’s Perspective on NF2-SWN

Perspectives of Adult Patients and Caregivers on the Management and Challenges Associated with Neurofibromatosis Type 1 and Plexiform Neurofibromas: A Multinational Qualitative Survey

Surgical Correction of Severe Dystrophic Cervical Kyphosis With Intraoperative Motor-Evoked Potential Changes in a Pediatric Patient With Neurofibromatosis Type 1

NF2 related schwannomatosis affects everyone differently. It’s a genetic condition that causes tumours to grow on nerves in the brain, inner ear, spinal cord, or peripheral nerves. it can be truly life changing. Learn more at curenf2.org. #endNF2 #NF2awarene

Lisch Nodules: Small, dome-shaped, well-defined tan to brown raised spots on the surface of the iris, typically multiple, smooth, and visible on slit-lamp eye exam rather than to the naked eye. The academy tells us this automatically points to neurofibromatosi

Image credit: Adams EG, Stewart KM, Borges OA, Darling T. Multiple, unilateral lisch nodules in the absence of other manifestations of neurofibromatosis type 1. Case Rep Ophthalmol Med. 2011;2011:854784. Epub 2012 Jan 23. PMID: 22606479; PMCID: PMC3350217. do

Cherry angiomas occurred more frequently in patients with #neurofibromatosis type 1 compared with control patients at rates of 48% vs 18%. Read more: https://www.dermatologyadvisor.com/news/cherry-angiomas-may-be-unrecognized-manifestation-neurofibromatosis-1

wanted to update Salems ref a bit to include something apart of my life and very personal to me. I was born with something called neurofibromatosis type 1 and #Danganronpa #DanganronpaOC

statistically I wonder what are the odds of me being the ONLY person with neurofibromatosis in any of the fandoms I’m in like,,, there’s gotta be SOMEONE else right? 🤔 especially in larger fandoms like pokemon

Attention-deficit/hyperactivity disorder in neurofibromatosis type 1

Palatine NF Walk raises support for neurofibromatosis research - Yahoo

Children's Tumor Foundation's NF Walk in Palatine raises awareness and support for neurofibromatosis research - ABC7 Chicago

Neurocutaneous Syndromes in Children: Prevalence and Clinical Characteristics [NOT_YET_RECRUITING]

Natural History and Biology of Skin Neurofibromas in Neurofibromatosis Type 1 [COMPLETED]

AZD6244 Hydrogen Sulfate for Children With Nervous System Tumors [ACTIVE_NOT_RECRUITING]

Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial) [ACTIVE_NOT_RECRUITING]

Targeted Therapy Directed by Genetic Testing in Treating Patients With Locally Advanced or Advanced Solid Tumors, The ComboMATCH Screening Trial [RECRUITING]

Natural History Study of Patients With Neurofibromatosis Type I [ACTIVE_NOT_RECRUITING]

WATCH 🎥: Rebecca Brown, MD, discusses how the NCCN guideline inclusion of brigatinib is changing clinical practice for NF2-related schwannomatosis. #oncology www.onclive.com/view/dr-brow...

NF2 related schwannomatosis affects everyone differently. It’s a genetic condition that causes tumours to grow on nerves in the brain, inner ear, spinal cord, or peripheral nerves, it can be truly life changing. Learn more at curenf2.org. #endNF2 #NF2awarenes

Palatine NF Walk raises awareness, support for neurofibromatosis research