Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain‐of‐function A391E mutation in FGFR3 gene-Reference-Cited by-同舟云学术

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Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain‐of‐function A391E mutation in FGFR3 gene

Published:2020-08-29 Issue:12 Volume:47 Page:
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Kariya Hitomi¹²,Nakano Hajime³,Ishii Naomi⁴,Kaimi Yuto⁴,Imai Keisuke⁵,Nakanishi Yoko⁶,Kunihiro Noritsugu⁶,Fukai Kazuyoshi¹^ORCID

Affiliation:

1. Department of Dermatology Osaka City General Hospital OsakaJapan

2. Education Training Center Osaka City General Hospital OsakaJapan

3. Department of Dermatology Hirosaki University Graduate School of Medicine HirosakiJapan

4. Department of Pathology Osaka City General Hospital OsakaJapan

5. Department of Plastic Surgery Osaka City General Hospital OsakaJapan

6. Department of Pediatric Neurosurgery Osaka City General Hospital OsakaJapan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15580

Reference5 articles.

1. Crouzonʼs Syndrome Associated with Acanthosis Nigricans: Ramifications for the Craniofacial Surgeon

2. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

3. Growth Regulation in Normal and Malignant Melanocytes

4. Familial acanthosis nigricans with the FGFR3 mutation: Differences of pigmentation between male and female patients

5. Reactivation of Mitogen-activated Protein Kinase (MAPK) Pathway by FGF Receptor 3 (FGFR3)/Ras Mediates Resistance to Vemurafenib in Human B-RAF V600E Mutant Melanoma

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acanthosis Nigricans: An Updated Review;Current Pediatric Reviews;2023-02

2. Crouzon syndrome with acanthosis nigricans: A case report and literature review;Dermatology Reports;2022-12-23

3. FGFR2 Mutation p.Cys342Arg Enhances Mitochondrial Metabolism-Mediated Osteogenesis via FGF/FGFR-AMPK-Erk1/2 Axis in Crouzon Syndrome;Cells;2022-10-05

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