A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome

A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome

Introduction: Vulto-van Silfhout-de Vries Syndrome (VSVS; OMIM#615828) is a rare hereditary disease associated with impaired intellectual development and speech, delayed psychomotor development, and behavioral anomalies, including autistic behavioral traits and poor eye contact. To date, 27 patients...

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Bibliographic Details
Main Authors: Natalia Bodunova, Maria Vorontsova, Igor Khatkov, Elena Baranova, Svetlana Bykova, Daniil Degterev, Maria Litvinova, Airat Bilyalov, Maria Makarova, Olesya Sagaydak, Anastasia Danishevich
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Diagnostics
Subjects:
VULTO-VAN syndrome
<i>DEAF1</i>
VSVS
Online Access:https://www.mdpi.com/2075-4418/12/8/1887

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