A Saudi Infant with Vici Syndrome: Case Report and Literature Review

INTRODUCTION: Vici syndrome, a rare autosomal recessive disorder, was first described in 1988 by Vici et al. Only 78 cases have been reported to date. The syndrome is characterised by agenesis of the corpus callosum, hypopigmentation, cardiomyopathy, progressive failure to thrive, dysmorphic feature...

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Detalles Bibliográficos
Autores principales: Alzahrani, Alhussain, Alghamdi, Abdulrahman Abdullah, Waggass, Rahaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Republic of Macedonia 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026433/
https://www.ncbi.nlm.nih.gov/pubmed/29983806
http://dx.doi.org/10.3889/oamjms.2018.271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026433/
https://www.ncbi.nlm.nih.gov/pubmed/29983806
http://dx.doi.org/10.3889/oamjms.2018.271

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