Port‐wine stains associated with large vestibular aqueduct syndrome caused by mutations in GNAQ and SLC26A4 genes: A case report
Author:
Affiliation:
1. Department of Dermatology West China Hospital Sichuan University Chengdu China
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15130
Reference10 articles.
1. Update on Sturge–Weber Syndrome: Diagnosis, Treatment, Quantitative Measures, and Controversies
2. Sturge-Weber Syndrome in Patients with Facial Port-Wine Stain
3. Facial port-wine stains – clinical stratification and risks of neuro-ocular involvement
4. Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
5. Vertical parasagittal hemispherotomy for Sturge–Weber syndrome in early infancy: case report and literature review
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1. GNAQ mutations drive port wine birthmark-associated Sturge-Weber syndrome: A review of pathobiology, therapies, and current models;Frontiers in Human Neuroscience;2022-11-03
2. Whole-Genome Sequencing Identified KCNJ12 and SLC25A5 Mutations in Port-Wine Stains;Frontiers in Medicine;2022-07-20
3. Acute effect of a variable pulse width Nd:YAG laser combined with hematoporphyrin monomethyl ether-mediated photodynamic therapy on a cockscomb model of nevus flammeus;Advances in Clinical and Experimental Medicine;2020-12-31
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