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

  • 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

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

Figure 3

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

Affected individualsNormal reference range
Clinical featuresII-1II-2
Sexfemalemale
Age(at first diagnosis of diabetes)3433
Height (cm)162N/A
Weight (kg)5445
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)40.2214.913.89-6.4
 HbA1c %13.89.0<6.4
 Islet beta-cell autoantibodiesN/A
 HOMA-β (%)4.6321.69
 IGF-1 (ng/ml)N/A43115-320
 Hb (g/L)81105115-150
 PLT (G/L)6389125-250
Sexual hormonesMaleFemale (follicular phase)
 Progesterone (ng/ml)0.20.20.10-0.30
 FSH (mIU/ml)4.230.990.95-11.953.03-8.08
 PRL (ng/ml)11.175.43.46-19.405.18-26.53
 Estradiol (pg/ml)201411-4421-251
 Testosterone (nmol/l)1.60.894.94-32.010.38-1.97
 LH (mIU/ml)0.780.161.14-8.752.39-6.60
ECG abnormalities++

Clinical features of affected individuals in the family.

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.

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.

Summary

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

Volume

13 - 2022

Updates

Copyright

*Correspondence: Huiqing Li,

†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

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.

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