GNB1 haploinsufficiency presents as monogenic obesity syndrome

Artikel in diesem Heft

1. Frontmatter
2. Mini Review
3. Transition of care from childhood/adolescence to adulthood in familial hypercholesterolemia
4. Original Articles
5. Performance of adult height prediction methods in 6 to 8-year-old girls with GnRH-dependent precocious puberty
6. Height velocity in the detection of growth disorders reconsidered: a retrospective analysis of the DONALD study
7. Differentiating transient and permanent congenital hypothyroidism: predictive clues from Istanbul, Türkiye
8. Evaluation of thyrotrophic and lactotrophic reserves in patients with pituitary dwarfism with and without empty sella turcica
9. Exploring the impact of androgen levels on depression and anxiety in adolescent females: a clinical perspective
10. The diagnostic value of stimulated androgen ratios in 5-alpha reductase type 2 (SRD5A2) deficiency: a case series and review of the literature
11. Prolonged symptom duration and the potential for gradual progression in pediatric adrenocortical tumors: observations from the MET studies
12. Distinguishing organic from idiopathic central precocious puberty: clinical characteristics and predictive factors for organic etiology in a multicenter Italian cohort study
13. Endocrinopathies associated with pediatric common variable immunodeficiency
14. Genetic, neuroimaging, and clinical characteristics of a cohort of individuals with L-2-hydroxyglutaric aciduria from Türkiye
15. Short Communications
16. Stress hyperglycemia in pediatric patients as a risk factor for type 1 diabetes – a single center experience
17. Observations of the effect of gonadotropin-releasing hormone analog treatment on psychosocial well-being in transgender youth and their caregivers – a pilot study
18. Letter to the Editor
19. GNB1 haploinsufficiency presents as monogenic obesity syndrome
20. Case Reports
21. Rare pediatric insulinoma case diagnosed by endoscopic ultrasonography: insights into endogenous hyperinsulinemic hypoglycemia
22. Caudal epidural steroid injection as a novel therapy for treatment-induced neuropathy of diabetes in children: report of two cases
23. A novel homozygous missense DNAJC3 variant in syndromic juvenile-onset diabetes
24. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: case report of a child with rare HMGCL gene variants