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Tooth transplantation in cherubism and incontinentia pigmenti: report of two unusual cases

✍ Scribed by J.L. Jensen; B. Album

Book ID
111430131
Publisher
Wiley (Blackwell Publishing)
Year
2010
Tongue
English
Weight
602 KB
Volume
4
Category
Article
ISSN
1752-2471

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Familial incontinentia pigmenti (IP) is a rare X-linked dominant disorder that affects ectodermal tissues. Over 90% of IP carrier females have a recurrent genomic deletion of exons 4-10 of the NEMO (IKBKG-IKKgamma) gene, which encodes a regulatory component of the IkB kinase complex, required to act