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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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Podrobná bibliografie
Vydáno v:Int Med Case Rep J
Hlavní autoři: Saeidi, Minoo, Shahbandari, Morteza
Médium: Artigo
Jazyk:Inglês
Vydáno: Dove 2020
Témata:
On-line přístup: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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