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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove
2020
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| 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 |