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Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy
The frequency of 18p deletion syndrome is estimated to be ∼1/50,000 live births and is more commonly associated with certain clinical features including short stature, intellectual disability, and facial dysmorphism. Physical examination of our patient revealed a short stature, intellectual disabili...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Georg Thieme Verlag KG
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192171/ https://www.ncbi.nlm.nih.gov/pubmed/35707779 http://dx.doi.org/10.1055/s-0042-1743261 |