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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Detalles Bibliográficos
Autores principales: Bodunova, Natalia, Vorontsova, Maria, Khatkov, Igor, Baranova, Elena, Bykova, Svetlana, Degterev, Daniil, Litvinova, Maria, Bilyalov, Airat, Makarova, Maria, Sagaydak, Olesya, Danishevich, Anastasia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406734/
https://www.ncbi.nlm.nih.gov/pubmed/36010237
http://dx.doi.org/10.3390/diagnostics12081887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406734/
https://www.ncbi.nlm.nih.gov/pubmed/36010237
http://dx.doi.org/10.3390/diagnostics12081887

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