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Pallister-Killian Mosaic Syndrome in an Omani Newborn: A Case Report and Literature Review
Pallister-Killian mosaic syndrome (PKS) is a rare sporadic condition with multiple congenital anomalies and intellectual deficits caused by mosaic tissue-limited tetrasomy of the short arm of chromosome 12 (12p). The clinical features are highly variable, ranging from mild to severe. Diagnosis is us...
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| Publicado no: | Oman Med J |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
OMJ
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6505352/ https://ncbi.nlm.nih.gov/pubmed/31110634 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5001/omj.2019.47 |
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