Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma-Reference-Cited by-同舟云学术

Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma

Published:2020-03-27 Issue:6 Volume:47 Page:
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Kantaputra Piranit¹²^ORCID,Intachai Worrachet¹,Kawasaki Katsushige³,Ohazama Atsushi³,Carlson Bruce⁴,Quarto Natalina⁵,Pruksachatkun Chulabhorn⁶,Chuamanochan Mati⁷^ORCID

Affiliation:

1. Division of Pediatric Dentistry Department of Orthodontics and Pediatric Dentistry Faculty of Dentistry Chiang Mai University Chiang Mai Thailand

2. Dentaland Clinic Chiang Mai Thailand

3. Division of Oral Anatomy Department of Oral Biological Science Niigata University Graduate School of Medical and Dental Sciences Niigata Japan

4. Department of Anatomy and Cell Biology University of Michigan Ann Arbor Michigan USA

5. Division of Plastic and Reconstructive Surgery Department of Surgery Stanford University School of Medicine Stanford California USA

6. Division of Pediatric Dermatology Department of Pediatrics Faculty of MedicineChiang Mai University Chiang Mai Thailand

7. Division of Dermatology Department of Internal Medicine Chiang Mai University Chiang Mai Thailand

Funder

Thailand Research Fund

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15333

Reference5 articles.

1. Pterygium and thinning of nails as an unusual manifestation in Clouston syndrome

2. Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma

3. WNT10B mutations associated with isolated dental anomalies

4. GJB6, of which mutations underlie Clouston syndrome, is a potential direct target gene of p63

5. Heterozygous Mutation in the SAM Domain of p63 Underlies Rapp-Hodgkin Ectodermal Dysplasia

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. Inherited Hair Disorders;Rook's Textbook of Dermatology;2024-02-20

2. A novel variant in the GJB6 gene in a large Chinese family with a unique phenotype of Clouston syndrome;Frontiers of Medicine;2023-01-16

3. Pili Torti: A Feature of Numerous Congenital and Acquired Conditions;Journal of Clinical Medicine;2021-08-30