Correction: Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study - Report - MDSpire

Correction: Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study

  • By

  • Lourdes Vega-Hannah

  • Mario Sanz-Cuesta

  • Didac Casas-Alba

  • Mercé Bolasell

  • Loreto Martorell

  • Leticia Pías

  • Ana Lucia Feller

  • Antonio F. Martinez-Monseny

  • Mercedes Serrano

  • June 2, 2026

  • 0 min

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Clinical Report: Correction on Sotos Syndrome Phenotypic Spectrum Study

Overview

This report corrects author names and acknowledges equal contributions in a study on Sotos syndrome involving 31 individuals. The original publication has been updated to reflect these changes.

Background

Sotos syndrome is characterized by overgrowth and intellectual disability, primarily caused by NSD1 gene mutations. Understanding its phenotypic spectrum is crucial for accurate diagnosis and management. Recent studies have expanded the recognized clinical features and associated comorbidities, emphasizing the need for ongoing research in this area.

Data Highlights

No numerical or trial data is presented in the correction article.

Key Findings

  • Correction of author names in the original publication.
  • Inclusion of an equal contribution statement for two authors.
  • Updated author list reflects the accurate contributions to the study.
  • The original article has been revised to correct these errors.

Clinical Implications

Accurate authorship and contribution acknowledgment are essential for maintaining the integrity of scientific literature. This correction highlights the importance of transparency in research collaborations.

Conclusion

The correction ensures that the contributions of all authors are properly recognized, which is vital for the credibility of the research on Sotos syndrome.

Related Resources & Content

  1. Vega-Hanna L, Sanz-Cuesta M, et al., Front. Pediatr., 2023 -- Correction: Expanding the Phenotypic Spectrum of Sotos Syndrome
  2. The Journal of Clinical Endocrinology & Metabolism — Phenotypic Associations with SOX9 Upstream Duplications: Advancements in Understanding Clinical Presentation and Diagnosis
  3. Brain — Spectrum of Genotypes and Phenotypes in Charcot-Marie-Tooth Disease Associated with SORD Mutations
  4. Clinical Rheumatology — Whole genome sequencing reveals genetic variants linked to sarcoidosis in a family with a notable incidence of the disease
  5. The Journal of Clinical Endocrinology & Metabolism — Broadening the Understanding of Endocrine Disorders Linked to SOX11 Variants
  6. Sotos Syndrome - GeneReviews® - NCBI Bookshelf
  7. Sotos Syndrome: Deep Neuroimaging Phenotyping Reveals a High Prevalence of Malformations of Cortical Development - PubMed

Original Source(s)

Correction: Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study

  • by Lourdes Vega-Hannah, Mario Sanz-Cuesta, Didac Casas-Alba, Mercé Bolasell, Loreto Martorell, Leticia Pías, Ana Lucia Feller, Antonio F. Martinez-Monseny, Mercedes Serrano

  • June 2, 2026

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