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Chu et al. Rare Dis Orphan Drugs J 2023;2:15 Rare Disease and
DOI: 10.20517/rdodj.2023.28
Orphan Drugs Journal

Correction Open Access

Correction: A report and review of the recurrent
c.811C > T variant and mutation spectrum of Kindler

syndrome in East Asians: a diagnostic odyssey of 2
weeks versus 49 years

3
1
1,#
1
2,#
Annie Tsz Wai Chu , Joshua Chun Ki Chan , Jasmine Lee Fong Fung , Wenshu Tang , Mianne Lee , Sze
2
2
4
3
4
Man Wong , Man Ho Chung , Geoffrey Yu , Vivien Li , Calvin Tik Hei Ng , Hong Kong Genome Project,
Brian Hon Yin Chung 1,3
1
Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
2
Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region, Hong
Kong, China.
3
Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The
University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
4
Division of Dermatology, Department of Medicine, Clinical School of Medicine, The University of Hong Kong, Hong Kong, China.
#
Authors contributed equally and considered joint first authors.
Correspondence to: Dr. Brian Hon Yin Chung, Hong Kong Genome Institute, 2/F, Building 20E, Hong Kong Science Park, Hong
Kong, China. E-mail: bhychung@genomics.org.hk
How to cite this article: Chu ATW, Chan JCK, Fung JLF, Tang W, Lee M, Wong SM, Chung MH, Yu G, Li V, Ng CTH, Project
HKG, Chung BHY. Correction: A report and review of the recurrent c.811C > T variant and mutation spectrum of Kindler
syndrome in East Asians: a diagnostic odyssey of 2 weeks versus 49 years. Rare Dis Orphan Drugs J 2023;2:15.
https://dx.doi.org/10.20517/rdodj.2023.28
Received: 14 Aug 2023 Accepted: 18 Aug 2023 Published: 21 Aug 2023
Academic Editor: Daniel Scherman Copy Editor: Dan Zhang Production Editor: Dan Zhang
The Case Report was published on 3 Mar 2023.

The authors wish to add Dr. Sze Man Wong as a co-author of the paper and add the Authors’ contributions
in the Declaration part of the paper. The two cases reported in the paper were under Dr Wong’s care. The
dermatological symptoms and signs are under vigorous dermatological verification by her, together with
initiating a referral for a genetic test, as in these two reported cases. She provided details of the
dermatological description, reflecting the expert input after that by dermatologists.
The authors apologize for any inconvenience caused and state that the scientific conclusions are unaffected.

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