Correction: Central precocious puberty as the initial manifestation of multisystem involvement caused by de novo heterozygous KMT2B mutation and STS hemizygous deletion: a case report - Summary - MDSpire
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Correction: Central precocious puberty as the initial manifestation of multisystem involvement caused by de novo heterozygous KMT2B mutation and STS hemizygous deletion: a case report
To correct errors in the previously published case report regarding central precocious puberty as the first sign of multisystem involvement due to a de novo heterozygous KMT2B mutation.
Approach:
Correction of References: Updated references in Table 2 for Forzano F et al. from '30' to '31' and for Li XY et al. from '31' to '32'.
Correction of Reference Range: Corrected the reference range for inhibin B from '27.06-8.96 pg/mL' to '27.06-48.96 pg/mL'.
Correction in Case Report: Updated the case report section to reflect that inhibin B was 217.58 pg/mL with the corrected reference range.
Key Findings:
Corrected reference citations in Table 2.
Updated the reference range for inhibin B.
Revised the case report section to include the accurate inhibin B measurement.
Interpretation:
The corrections ensure accurate representation of data and references in the context of KMT2B-related disorders.
Conclusion:
The original version of the article has been updated to reflect these corrections.
