Front. Pediatr. Frontiers in Pediatrics Front. Pediatr. 2296-2360 Frontiers Media S.A. 10.3389/fped.2020.624141 Pediatrics Correction Corrigendum: Overgrowth Syndromes—Evaluation, Diagnosis, and Management Manor Joshua * Lalani Seema R. Department of Molecular Genetics, Baylor College of Medicine, Houston, TX, United States *Correspondence: Joshua Manor manor@bcm.edu

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

This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Pediatrics

 23 12 2020 2020 8 624141 30 10 2020 17 11 2020 Copyright © 2020 Manor and Lalani. 2020 Manor and Lalani

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 Overgrowth Syndromes—Evaluation, Diagnosis, and Management by Manor, J., and Lalani, S. R. (2020). Front. Pediatr. 8:574857. doi: 10.3389/fped.2020.574857 overgrowth Beckwith-Wiedemann Simpson-Golabi-Behmel Sotos Weaver Pten PIK3CA Proteus Syndrome

In the original article, there was a mistake in Figure 3 as published. The permission for use of copyrighted material is not yet available to the authors. This figure has therefore been removed and referenced appropriately. Due to the removal of Figure 3, the figure numbering has been updated.

Additionally, in the original article, there was a mistake in Table 1 as published. The term “Exophthalmos” is incorrect, and should be replaced by the correct term, “Exomphalos.” The corrected Table 1 appears below.

Clinical diagnostic criteria for Beckwith–Wiedemann syndrome.

Feature Pts
Cardinal findings
Macroglossia 2
Exomphalos 2
Lateralized overgrowth 2
Multifocal and/or bilateral Wilms tumor 2
Persistent hyperinsulinism (> 1 week) 2
Characteristic pathology: adrenal cortex cytomegaly, placental mesenchymal dysplasia, pancreatic adenomatosis 2
Minor findings
Birthweight > 2 SD above the mean 1
Facial naevus simplex 1
Polyhydramnios 1
Ear creases and/or pits 1
Transient hyperinsulinism (<1 week) 1
Characteristic tumor: Unilateral Wilms tumor, neuroblastoma, rhabdomyosarcoma, hepatoblastoma, adrenocortical carcinoma, or pheochromocytoma 1
Nephromegaly and/or hepatomegaly 1
Umbilical hernia and/or diastasis recti 1
Interpretation:
Clinical score Diagnosis
4+ BWSp confirmed
2–3 Diagnosis by genetic testing
0–1 BWSp rejected

Adapted from Brioude et al. 2018.

There was one final error in the original article. “SET2D-related disorder” is incorrect, and this should be written as “SETD2-related disorder”. A correction has been made to Overgrowth Syndromes Presenting Prenatally, Sotos Syndrome, Paragraph 6: SETD2-related disorder is another example of a Sotos-like autosomal dominant overgrowth syndrome resulting in post-natal overgrowth, macrocephaly, prominent forehead, and advanced bone age, named Luscan-Lumish syndrome (OMIM 616831), (70), adding another layer of complexity to a diagnosis of Sotos syndrome based on clinical symptoms alone.

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