Mucocutaneous Findings and Endocrinopathies in Children with Turner Syndrome: A Cross-Sectional Study

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Authors: Selami Aykut Temiz, Filiz Cebeci, Aslıhan Çiçekli, Begüm Işık, Sevil Savaş Erdoğan, Selma Emre, Hilal Kaya Erdoğan, İsa An, Sezgi Sarıkaya Solak, Sevilay Oğuz Kiliç, Eda Öksüm Solak, Arzu Ataseven
+9 more Beray Selver Eklioğlu, Suna Kılınç, Mehmet Boyraz, Enver Şimşek, Tuğba Kontbay, Filiz Tütüncüler, Durmuş Doğan, Ülkü Gül Şıraz, Güllü Eren
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Abstract

Objective: To investigate the frequency of skin, hair, nail, and mucosal findings in children with Turner syndrome (TS) and their associations with coexisting endocrinopathies. Methods: A cross-sectional study was conducted with TS patients who were followed up by pediatric endocrinology and referred to the dermatology outpatient clinic. Data were collected using standardized dermatological examination forms, including demographic information, clinical features, presence of endocrinopathies, and medication usage. Statistical analysis was used to evaluate differences between groups and to analyze relationships between variables. Results: The cohort consisted of 112 girls with TS. Skin and hair findings were detected in 86.6% of the patients, with melanocytic nevi (44.6%) and xerosis (41.1%) being the most commonly observed. Oral mucosal findings were observed less frequently (17.0%). Nail findings were detected in 63.4% of the cases, with leukonychia (15.2%) and subungual hyperkeratosis (14.3%) being the most prevalent. Older age, delayed diagnosis, longer follow-up duration, and lower body mass index were associated with an increased frequency of skin and hair findings (p

Fields of Study & Subjects

Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities Sexual Differentiation and Disorders Genetic and rare skin diseases.

Publication details

Journal / source
Journal of Clinical Research in Pediatric Endocrinology
Volume
18
Issue
3
Pages
459–466
Publication date
26 February 2026
Language
EN