Incontinentia Pigmenti in a Newborn with NEMO Mutation

Incontinentia pigmenti (IP) (OMIM #308300) is a rare X-linked dominant neuroectodermal multisystemic syndrome due to mutations in the gene for NF-κB essential modulator (NEMO). A term newborn girl who was born with erythematous vesicular eruptions developed recurrent seizures during the first and se...

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Detaylı Bibliyografya
Asıl Yazarlar: Lee, Young, Kim, Sooyeon, Kim, Kyunghee, Chang, Meayoung
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Korean Academy of Medical Sciences 2011
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3031021/
https://ncbi.nlm.nih.gov/pubmed/21286028
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2011.26.2.308
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