- Incontinentia Pigmenti in a Newborn with NEMO Mutation
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Lee Y, Kim S, Kim K, Chang M
- KMID: 1782125
- J Korean Med Sci.
- 2011 Feb;26(2):308-311.
- doi: 10.3346/jkms.2011.26.2.308
Incontinentia pigmenti (IP) (OMIM #308300) is a rare X-linked dominant neuroectodermal multisystemic syndrome due to mutations in the gene for NF-kappaB essential modulator (NEMO). A term newborn girl who was... -
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- The Common NF-kappaB Essential Modulator (NEMO) Gene Rearrangement in Korean Patients with Incontinentia Pigmenti
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Song MJ, Chae JH, Park EA, Ki CS
- KMID: 2157858
- J Korean Med Sci.
- 2010 Oct;25(10):1513-1517.
- doi: 10.3346/jkms.2010.25.10.1513
Incontinentia pigmenti (IP) is a rare X-linked dominant disorder characterized by highly variable abnormalities of the skin, eyes and central nervous system. A mutation of the nuclear factor-kappa B essential... -
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