Related Experiment Video
Updated: Feb 21, 2026

An Orthotopic Sciatic Nerve Xenograft for Neurofibromatosis Type 1 Neurofibromas
Published on: October 10, 2025
[Lisch nodule in neurofibromatosis type 1]
Yassine Abaloun1, Yousra Ajhoun1
1Université Mohammed V Souissi, Service d'Ophtalmologie de l'Hôpital Militaire Mohamed V, Hay Riad, Rabat, Maroc.
Neurofibromatosis type 1 (NF1), a common genetic disorder, presents with varied symptoms. This case highlights Lisch nodules, characteristic iris tumors, as key ocular findings in an adult NF1 patient.
Area of Science:
- Genetics
- Ophthalmology
- Dermatology
Background:
- Neurofibromatosis type 1 (NF1), also known as Von Recklinghausen disease, is an autosomal dominant genetic disorder.
- NF1 is characterized by variable clinical manifestations, including cutaneous café-au-lait spots and neurofibromas, and can affect multiple organs.
- Ocular manifestations, particularly Lisch nodules (benign iris hamartomas), are common in NF1 and aid in diagnosis, especially in adults.
More Related Videos
08:57Author Spotlight: Genetically Engineered Mouse Models and Pathological Characterization of Neurofibromatosis Type 1 Associated Tumors
Published on: May 17, 2024
05:44Author Spotlight: Collecting the Brain and Serum from the Same Mice Fetus to Study Brain Tumor Development
Published on: May 17, 2024
Related Concept Videos
Neurulation
Neural Regulation
Notch Signaling Pathway
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...