# Novel Treatments, Approaches, Prevention Strategies, and Insights in Pediatric, Adolescent, and Gynecological Endocrinology

**Authors:** Dimitrios T. Papadimitriou

PMC · DOI: 10.3390/children12101358 · Children · 2025-10-09

## Full-text entities

- **Genes:** AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, GNAS (GNAS complex locus) [NCBI Gene 2778] {aka AHO, AIMAH1, C20orf45, GNAS1, GPSA, GSA}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, LHX1 (LIM homeobox 1) [NCBI Gene 3975] {aka LIM-1, LIM1}, WNT4 (Wnt family member 4) [NCBI Gene 54361] {aka SERKAL, WNT-4}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, HOXA@ (homeobox A cluster) [NCBI Gene 3197] {aka HOX1@}, CCDC134 (coiled-coil domain containing 134) [NCBI Gene 79879] {aka OI22}, TRH (thyrotropin releasing hormone) [NCBI Gene 7200] {aka Pro-TRH, TRF}, INHBE (inhibin subunit beta E) [NCBI Gene 83729], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, FST (follistatin) [NCBI Gene 10468] {aka FS}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}
- **Diseases:** Cancer (MESH:D009369), chromosomal abnormalities (MESH:D002869), Perimenstrual Asthma (MESH:D001249), Osteogenesis Imperfecta (MESH:D010013), Ehlers-Danlos syndrome (MESH:D004535), Inflammation (MESH:D007249), Pseudohypoparathyroidism (MESH:D011547), injury to (MESH:D014947), Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome (MESH:C537371), Thyroid Microcarcinoma (MESH:C563277), Genetic Disorders (MESH:D030342), Amenorrhea (MESH:D000568), Obesity (MESH:D009765), Fetal Fractures (MESH:D005315), infertility (MESH:D007246), Endocrine and Metabolic Disorders (MESH:D004700), Primary (MESH:D010538), iodine deficiency (MESH:D003409), Androgen Insensitivity Syndrome (MESH:D013734), Hypocalcemia (MESH:D006996), Spina Bifida (MESH:D016135), leukocyte adhesion deficiency (MESH:C535887), Breast Anomalies (MESH:D061325), PCOS (MESH:D011085), proliferative breast disease (MESH:D001941), Li-Fraumeni Syndrome (MESH:D016864)
- **Chemicals:** estradiol (MESH:D004958), Vitamin D (MESH:D014807), phosphate (MESH:D010710), homocysteine (MESH:D006710), calcium (MESH:D002118), inositol (MESH:D007294)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Ala871Glu

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12563840/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12563840/full.md

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Source: https://tomesphere.com/paper/PMC12563840