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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Korean Academy of Medical Sciences
2011
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| Matèries: | |
| Accés en línia: | 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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