CORRECTION article

Front. Endocrinol., 21 February 2022

Sec. Clinical Diabetes

Volume 13 - 2022 | https://doi.org/10.3389/fendo.2022.856002

Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene

This article is a correction to:

  1. Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene

    1. Read original article
Min Zhou,&#x;Min Zhou1,2†Ningjie Shi,&#x;Ningjie Shi3,4†Juan Zheng,&#x;Juan Zheng3,4†Yang Chen,Yang Chen3,4Siqi Wang,Siqi Wang3,4Kangli Xiao,Kangli Xiao3,4Zhenhai Cui,Zhenhai Cui3,4Kangli Qiu,Kangli Qiu3,4Feng Zhu,Feng Zhu5,6Huiqing Li,*Huiqing Li3,4*
  • 1Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 2Key Laboratory of Respiratory Diseases, National Ministry of Health of the People’s Republic of China and National Clinical Research Center for Respiratory Disease, Wuhan, China
  • 3Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 4Hubei Provincial Clinical Research Center for Diabetes and Metabolic Disorders, Wuhan, China
  • 5Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 6Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

A Corrigendum on:
Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene

By Zhou, M., Shi, N., Zheng, J., Chen, Y., Wang, S., Xiao, K., Cui, Z., Qiu, K., Zhu, F. and Li, H. (2021) Front. Endocrinol. 12:770871. doi: 10.3389/fendo.2021.770871

In the article as published originally, there was a typographical error in the caption for Figure 3B.

FIGURE 3
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Figure 3 The images of the WSS patients. (A) Computed tomography of the abdomen of the proband demonstrated atrophy of the pancreas. (B) Computed tomography of the abdomen of the brother of proband showed uneven pancreatic density. (C, D) Pituitary MR of the brother of proband indicated the empty sella and none pituitary gland. (E) Hip CT of the brother of proband suggested osteoporosis that was not consistent with actual age. (arrows).

The sentence “Computed tomography of the, bdomen of the brother of proband showed uneven pancreatic density” should be “Computed tomography of the abdomen of the brother of proband showed uneven pancreatic density”.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

In the article as published originally, there was a typographical error in Table 1. The normal reference range for IGF-1 was incorrectly presented as “115-323 ng/ml”; the correct adult reference range is “115-320 ng/ml”.

TABLE 1
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Table 1 Clinical features of affected individuals in the family.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

In the article as published originally, there was a typographical error in the section Case Description, subsection Case 2. The IGF-1 range for Case 2 was incorrectly presented as “111-549 ng/ml”; the correct adult reference range is “115-320 ng/ml”.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: Woodhouse–Sakati syndrome, diabetes, intellectual disability, alopecia, hypogonadism

Citation: Zhou M, Shi N, Zheng J, Chen Y, Wang S, Xiao K, Cui Z, Qiu K, Zhu F and Li H (2022) Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene. Front. Endocrinol. 13:856002. doi: 10.3389/fendo.2022.856002

Received: 16 January 2022; Accepted: 25 January 2022;
Published: 21 February 2022.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2022 Zhou, Shi, Zheng, Chen, Wang, Xiao, Cui, Qiu, Zhu and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Huiqing Li, bGhxaW5nNUAxMjYuY29t

†These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.