The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti

Incontinentia pigmenti (IP) is a rare skin disease combined with anomalies of the teeth, eyes, and central nervous system (CNS). Mutations of the IKBKG gene are responsible for IP. Among the most frequent CNS abnormalities found in IP using magnetic resonance imaging (MRI) are corpus callosum (CC) a...

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Detalles Bibliográficos
Autores principales: Minić, Snežana, Cerovac, Nataša, Novaković, Ivana, Gazikalović, Slobodan, Popadić, Svetlana, Trpinac, Dušan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093331/
https://www.ncbi.nlm.nih.gov/pubmed/37046518
http://dx.doi.org/10.3390/diagnostics13071300

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093331/
https://www.ncbi.nlm.nih.gov/pubmed/37046518
http://dx.doi.org/10.3390/diagnostics13071300

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