ORAL AND DENTAL FINDINGS OF A CHILD WITH WEILL-MARCHESANI SYNDROME TYPE II: A CASE REPORT WITH 3-YEAR FOLLOW-UP

Weill-Marchesani syndrome (WMS, OMIM# 227600) is a genetically determined, rare systemic connective tissue disorder. The syndrome is divided into four types according to mutations in related genes. Given the limited number of individuals with WMS in the literature, no genotype-phenotype correlations...

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Váldodahkkit:	Melike Tıraş, Muhsin Elmas, Burcu Güçyetmez Topal
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Selcuk University Press 2023-06-01
Ráidu:	Selcuk Dental Journal
Fáttát:	dental anomaliler fbn-1 gen mutasyonu weill-marchesani sendromu dental anomalies fnb-1 gene mutation weill-marchesani syndrome
Liŋkkat:	https://dergipark.org.tr/tr/download/article-file/2880593
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