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Familial, constitutional, and combined idiopathic short stature: longitudinal growth patterns and pubertal effects

BackgroundPathological causes account for approximately 15%–20% of short-stature cases, whereas about 80% of short-statured children have no identifiable underlying etiology and are classified as idiopathic short stature (ISS). ISS represents a highly heterogeneous group, and ongoing debates persist...

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Principais autores: Erkut Gürlek, Sirmen Kızılcan Çetin, Elif Özsu, Zehra Aycan, Merih Berberoğlu, Zeynep Şıklar
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2026-03-01
Serier:Frontiers in Pediatrics
Fag:
bone age
constitutional delay
familial short stature
growth velocity
idiopathic short stature
puberty
Online adgang:https://www.frontiersin.org/articles/10.3389/fped.2026.1783065/full
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