# Editorial: Stars and rising stars in pediatric endocrinology: 2022

**Authors:** Benjamin Udoka Nwosu

PMC · DOI: 10.3389/fendo.2024.1384549 · Frontiers in Endocrinology · 2024-03-18

## Full-text entities

- **Genes:** CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, ABRA (actin binding Rho activating protein) [NCBI Gene 137735] {aka STARS}
- **Diseases:** autosomal recessive disease (MESH:D030342), GH deficiency (MESH:D004393), optic atrophy (MESH:D009896), hyperglycemic (MESH:D006944), malignancies (MESH:D009369), insulinoma (MESH:D007340), diabetes (MESH:D003920), hyperinsulinemic hypoglycemia (MESH:D044903), endocrine disorders (MESH:D004700), WS (MESH:D014929), pancreatic tumors (MESH:D010190), atherosclerotic cardiovascular disease (MESH:D050197), deafness (MESH:D003638), COVID-19 (MESH:D000086382), WSS (OMIM:605130), glycogen storage diseases (MESH:D006008), non-autoimmune diabetes mellitus (MESH:C565730), multiple endocrine neoplasia type 1 (MEN 1) syndrome (MESH:D018761), DSD (MESH:D012734), CPP (MESH:D011629), hormone-secreting tumors (MESH:D049912), dyslipidemia (MESH:D050171), DSDs (MESH:D058533), short stature (MESH:D006130), T1D. (MESH:D003922), diabetes insipidus (MESH:D003919), cystic fibrosis (MESH:D003550), hypergonadotropic hypogonadism (MESH:D007006)
- **Chemicals:** glucose (MESH:D005947), 11-ketotestosterone (MESH:C003600), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC10982425/full.md

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Source: https://tomesphere.com/paper/PMC10982425