Genetic and Clinical Data for Pediatric Congenital Hypothyroidism Patients

Supplementary data for a study on DUOX2 mutations in congenital hypothyroidism contains de-identified clinical and genetic tables for pediatric patients. The 22.8 KB XLSX file includes patient IDs, thyroid morphology, thyroid function indicators, follow-up lab data, and genetic mutation profiles. Authored by Feng Cheng and last updated in May 2026, it supports the statistical analysis of the associated manuscript.

Use Cases

• Correlate specific DUOX2 mutations with thyroid morphological features based on the described genetic mutation profiles.
• Analyze the relationship between baseline thyroid function indicators and long-term outcomes based on the latest follow-up laboratory data.
• Train models to predict clinical severity from genetic profiles based on the combined clinical and genetic variables.

Strengths

• Data is explicitly de-identified for academic sharing, protecting patient privacy.
• Includes longitudinal data with baseline and follow-up clinical measurements.
• Focuses on a specific genetic cause (DUOX2) of a well-defined medical condition.

Limitations

• The dataset is very small at 22.8 KB, indicating a limited sample size.
• Row count and column-level documentation are unknown, requiring manual inspection after download.
• Data may reflect temporal and source bias inherent to the single associated study.

Provenance

Source

Feng Cheng via figshare.

Collection Method

Collected as part of a clinical research study on congenital hypothyroidism.

Freshness

Last updated 2026-05-13 06:49:33.