Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center

INTRODUCTION: Narcolepsy Type 1 (NT1) is a rare hypersomnia of central origin linked to hypocretin deficiency, most frequently arising at pediatric age. NT1 could be associated with endocrine comorbidities involving the neuroendocrine axis, predominantly obesity, and Central Precocious Puberty (CPP)...

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Detalles Bibliográficos
Autores principales: Casale, Sara, Assirelli, Valentina, Pizza, Fabio, Balsamo, Antonio, Gennari, Monia, Pession, Andrea, Plazzi, Giuseppe, Cassio, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311432/
https://www.ncbi.nlm.nih.gov/pubmed/37396177
http://dx.doi.org/10.3389/fendo.2023.1037398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311432/
https://www.ncbi.nlm.nih.gov/pubmed/37396177
http://dx.doi.org/10.3389/fendo.2023.1037398

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