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Neuroimaging findings in Pallister-Killian syndrome
Pallister-Killian syndrome (PKS) is a rare chromosomal duplication disorder caused by additional copies of the short arm of chromosome 12 (12p). Clinically PKS is characterized by craniofacial dysmorphism with neonatal frontotemporal alopecia, hypertelorism, and low-set ears as well as kyphoscoliosi...
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| Publicado en: | Neuroradiol J |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
SAGE Publications
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6111437/ https://ncbi.nlm.nih.gov/pubmed/29260614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400917744798 |
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