A Child with Seckel Syndrome and Arterial Stenosis: Case Report and Literature Review

BACKGROUND: Seckel syndrome is a rare genetic disorder with autosomal recessive inheritance. It is characterized by dysmorphic features, intrauterine and postnatal growth restriction, microcephaly and mental retardation. Although cardiovascular complications are not prevalent in this syndrome, sever...

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Detalles Bibliográficos
Autores principales: Saeidi, Minoo, Shahbandari, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234957/
https://www.ncbi.nlm.nih.gov/pubmed/32523383
http://dx.doi.org/10.2147/IMCRJ.S241601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234957/
https://www.ncbi.nlm.nih.gov/pubmed/32523383
http://dx.doi.org/10.2147/IMCRJ.S241601

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