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

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

IntroductionNarcolepsy 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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Bibliographic Details
Main Authors: Sara Casale, Valentina Assirelli, Fabio Pizza, Antonio Balsamo, Monia Gennari, Andrea Pession, Giuseppe Plazzi, Alessandra Cassio
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-06-01
Series:Frontiers in Endocrinology
Subjects:
narcolepsy type 1
obesity
central precocious puberty
final height
sodium oxybate
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2023.1037398/full

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https://www.frontiersin.org/articles/10.3389/fendo.2023.1037398/full

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