Artikel
Lizenziert
Nicht lizenziert
Erfordert eine Authentifizierung
Identification of pathogenic ACAN variants in healthy children with normal height and advanced bone age
-
María Isabel Hernández
, Vivian Gallardo
, Nancy Unanue , Hermine van Duyvenvoordeund María Verónica Mericq
Veröffentlicht/Copyright:
28. August 2025
Received: 2025-06-22
Accepted: 2025-08-09
Published Online: 2025-08-28
Published in Print: 2025-10-27
© 2025 Walter de Gruyter GmbH, Berlin/Boston
Sie haben derzeit keinen Zugang zu diesem Inhalt.
Sie haben derzeit keinen Zugang zu diesem Inhalt.
Artikel in diesem Heft
- Frontmatter
- Review
- A multi-stakeholder perspective on medical devices for children and adolescents with type 1 diabetes: huge unmet needs for the smallest
- Original Articles
- Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppression
- Testosterone in Duchenne muscular dystrophy: effects on puberty and growth
- First evaluation of fibroblast growth factor 21 levels in patients diagnosed with glycogen storage diseases with liver involvement
- Improving cardiometabolic health in children and adolescents with obesity: a comparison between in-person and virtual supervised training
- Impact of high-dose vitamin D supplementation initiated shortly after diagnosis on residual beta cell function and partial remission rates in children with type 1 diabetes
- Clinical spectrum, imaging characteristics, and treatment outcomes of pediatric adrenocortical tumors: a 24-year experience from Western India
- Comparison study of the correlation between free and total 25(OH)D in maternal and umbilical blood and early-life physical development parameters
- Hashimoto’s thyroiditis in children and adolescents: analysis of long-term course
- Case Reports
- 45, X/46, XY mosaicism and gender incongruence: ethical, medical, and psychological considerations
- Hormone-active ovarian steroid cell tumor in a 2-year-old girl
- Lipoatrophy following weekly growth hormone therapy: a case report
- Surgical treatment and somatostatin experience in growth hormone-secreting pituitary macroadenoma due to novel AIP mutation
- Letters to the Editor
- ANKS1B is a potential candidate gene for short stature and failure to thrive in children
- Identification of pathogenic ACAN variants in healthy children with normal height and advanced bone age
Artikel in diesem Heft
- Frontmatter
- Review
- A multi-stakeholder perspective on medical devices for children and adolescents with type 1 diabetes: huge unmet needs for the smallest
- Original Articles
- Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppression
- Testosterone in Duchenne muscular dystrophy: effects on puberty and growth
- First evaluation of fibroblast growth factor 21 levels in patients diagnosed with glycogen storage diseases with liver involvement
- Improving cardiometabolic health in children and adolescents with obesity: a comparison between in-person and virtual supervised training
- Impact of high-dose vitamin D supplementation initiated shortly after diagnosis on residual beta cell function and partial remission rates in children with type 1 diabetes
- Clinical spectrum, imaging characteristics, and treatment outcomes of pediatric adrenocortical tumors: a 24-year experience from Western India
- Comparison study of the correlation between free and total 25(OH)D in maternal and umbilical blood and early-life physical development parameters
- Hashimoto’s thyroiditis in children and adolescents: analysis of long-term course
- Case Reports
- 45, X/46, XY mosaicism and gender incongruence: ethical, medical, and psychological considerations
- Hormone-active ovarian steroid cell tumor in a 2-year-old girl
- Lipoatrophy following weekly growth hormone therapy: a case report
- Surgical treatment and somatostatin experience in growth hormone-secreting pituitary macroadenoma due to novel AIP mutation
- Letters to the Editor
- ANKS1B is a potential candidate gene for short stature and failure to thrive in children
- Identification of pathogenic ACAN variants in healthy children with normal height and advanced bone age