Prevalence of Endocrinopathies in a Cohort of Patients with Rett Syndrome: A Two-Center Observational Study.
CDKL5 deletion
MeCP2 deletion
Rett syndrome
endocrinopathy
epilepsy
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
24 Feb 2024
24 Feb 2024
Historique:
received:
23
01
2024
revised:
21
02
2024
accepted:
22
02
2024
medline:
28
3
2024
pubmed:
28
3
2024
entrez:
28
3
2024
Statut:
epublish
Résumé
Systematic data on endocrinopathies in Rett syndrome (RTT) patients remain limited and inconclusive. The aim of this retrospective observational two-center study was to assess the prevalence of endocrinopathies in a pediatric population of RTT patients. A total of 51 Caucasian patients (47 girls, 4 boys) with a genetically confirmed diagnosis of RTT were enrolled (mean age 9.65 ± 5.9 years). The patients were referred from the Rett Center of two Italian Hospitals for endocrinological evaluation. All the study population underwent clinical and auxological assessments and hormonal workups.
Identifiants
pubmed: 38540345
pii: genes15030287
doi: 10.3390/genes15030287
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM