Smith–Lemli–Opitz Syndrome: Oral Characteristics and Risk Factors for Caries Development

<b>Background/Objectives</b>: Smith–Lemli–Opitz syndrome is a metabolic autosomal recessive disease, characterized by congenital defects, with concomitant psychomotor developmental delay. The symptoms are variable and depend on the clinical form of the disease. The aim of this study was...

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Bibliographic Details
Main Authors: Dorota Olczak-Kowalczyk, Aneta Witt-Porczyk, Paula Piekoszewska-Ziętek, Małgorzata Krajewska-Walasek
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Biomedicines
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Online Access:https://www.mdpi.com/2227-9059/13/3/574
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