Front. Endocrinol. Frontiers in Endocrinology Front. Endocrinol. 1664-2392 Frontiers Media S.A. 10.3389/fendo.2022.856002 Endocrinology Correction Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene Zhou Min 1 2 † Shi Ningjie 3 4 † Zheng Juan 3 4 † Chen Yang 3 4 Wang Siqi 3 4 Xiao Kangli 3 4 Cui Zhenhai 3 4 Qiu Kangli 3 4 Zhu Feng 5 6 Li Huiqing 3 4 * 1 Department of Pulmonary and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China 2 Key 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 3 Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China 4 Hubei Provincial Clinical Research Center for Diabetes and Metabolic Disorders, Wuhan, China 5 Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China 6 Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

*Correspondence: Huiqing Li, lhqing5@126.com

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

This article was submitted to Clinical Diabetes, a section of the journal Frontiers in Endocrinology

 21 02 2022 2022 13 856002 16 01 2022 25 01 2022 Copyright © 2022 Zhou, Shi, Zheng, Chen, Wang, Xiao, Cui, Qiu, Zhu and Li 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.

 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 Woodhouse–Sakati syndrome diabetes intellectual disability alopecia hypogonadism

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

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”.

Clinical features of affected individuals in the family.

Affected individuals Normal reference range
Clinical features II-1 II-2
Sex female male
Age(at first diagnosis of diabetes) 34 33
Height (cm) 162 N/A
Weight (kg) 54 45
Clinical manifestations
 Alopecia + +
 Intellectual Disability + +
 Hypogonadism + +
 Diabetes Mellitus + +
 Anemia + +
 Thrombocytopenia + +
 Hypothyroidism – –
 Other Neurophysiology findings – –
 Sensorineural hearing loss – –
 Progressive extrapyramidal movements – –
 Laboratory tests
 Fasting blood glucose (mmol/L) 40.22 14.91 3.89-6.4
 HbA1c % 13.8 9.0 <6.4
 Islet beta-cell autoantibodies N/A –
 HOMA-β (%) 4.63 21.69
 IGF-1 (ng/ml) N/A 43 115-320
 Hb (g/L) 81 105 115-150
 PLT (G/L) 63 89 125-250
Sexual hormones Male Female (follicular phase)
 Progesterone (ng/ml) 0.2 0.2 0.10-0.30
 FSH (mIU/ml) 4.23 0.99 0.95-11.95 3.03-8.08
 PRL (ng/ml) 11.17 5.4 3.46-19.40 5.18-26.53
 Estradiol (pg/ml) 20 14 11-44 21-251
 Testosterone (nmol/l) 1.6 0.89 4.94-32.01 0.38-1.97
 LH (mIU/ml) 0.78 0.16 1.14-8.75 2.39-6.60
ECG abnormalities + +

HbA1c, Glycated hemoglobin; Hb, Hemoglobin; PLT, Platelet; FSH, Follicle-stimulating hormone; PRL, Prolactin; LH, Luteinizing hormone; ECG, Electrocardiographic; N/A, not available; +, positive; -, negative.

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.

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