Acanthosis nigricans, hypochondroplasia, and FGFR 3 mutations: Findings with five new patients, and a review of the literature

Author:

Muguet Guenot Louise1ORCID,Aubert Helene1,Isidor Bertrand2,Toutain Annick3,Mazereeuw‐Hautier Juliette4,Collet Corinne5,Bourrat Emmanuelle6,Denis Musquer Marie7,Barbarot Sébastien1,

Affiliation:

1. Department of Dermatology CHU Nantes Nantes France

2. Department of Genetics CHU Nantes Nantes France

3. Department of Genetics CHU Tours Tours France

4. Department of Dermatology CHU Toulouse Toulouse France

5. Department of Biochemistry APHP Hôpital Lariboisiêre Paris France

6. Department of Dermatology APHP Hôpital Saint‐Louis Paris France

7. Department of Pathology CHU Nantes Nantes France

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Cited by 6 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 and Hypochondroplasia Associated with FGFR3 Mutation;Indian Journal of Dermatology;2023-05

2. Hypochondroplasia with Acanthosis Nigricans and Moyamoya Disease;Annals of Child Neurology;2023-04-01

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

4. Growth Topics in FGFR3-Related Skeletal Dysplasias;Current Treatment Options in Pediatrics;2021-03-22

5. Acanthosis nigricans: A review;Journal of Cosmetic Dermatology;2020-07-16

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