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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
Publicado en:Int Med Case Rep J
Main Authors: Saeidi, Minoo, Shahbandari, Morteza
Formato: Artigo
Idioma:Inglês
Publicado: Dove 2020
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7234957/
https://ncbi.nlm.nih.gov/pubmed/32523383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IMCRJ.S241601
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