![IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male](https://www.mdpi.com/ijms/ijms-23-01179/article_deploy/html/images/ijms-23-01179-g003.png)
IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male
![IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male](https://pub.mdpi-res.com/ijms/ijms-23-01179/article_deploy/html/images/ijms-23-01179-g002.png?1643014884)
IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male
![A male infant with anhidrotic ectodermal dysplasia/immunodeficiency accompanied by incontinentia pigmenti and a mutation in the NEMO pathway. | Semantic Scholar A male infant with anhidrotic ectodermal dysplasia/immunodeficiency accompanied by incontinentia pigmenti and a mutation in the NEMO pathway. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/591e8bf155082e269bbc2c3543d11ea3944ad60b/4-Figure3-1.png)
A male infant with anhidrotic ectodermal dysplasia/immunodeficiency accompanied by incontinentia pigmenti and a mutation in the NEMO pathway. | Semantic Scholar
![Microdeletion / Duplication at the Xq 28 IP Locus Causes a De Novo IKBKG / NEMO / IKKgamma exon 4 _ 10 Deletion in Families with Incontinentia Pigmenti | Semantic Scholar Microdeletion / Duplication at the Xq 28 IP Locus Causes a De Novo IKBKG / NEMO / IKKgamma exon 4 _ 10 Deletion in Families with Incontinentia Pigmenti | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/192deb4b203fde5183139162e7999954bd9c67d7/2-Figure1-1.png)
Microdeletion / Duplication at the Xq 28 IP Locus Causes a De Novo IKBKG / NEMO / IKKgamma exon 4 _ 10 Deletion in Families with Incontinentia Pigmenti | Semantic Scholar
![Figure 1 from The Common NF-κB Essential Modulator (NEMO) Gene Rearrangement in Korean Patients with Incontinentia Pigmenti | Semantic Scholar Figure 1 from The Common NF-κB Essential Modulator (NEMO) Gene Rearrangement in Korean Patients with Incontinentia Pigmenti | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f8bf0fde79696bacc877b3ea0ec44e7baf915280/2-Figure1-1.png)
Figure 1 from The Common NF-κB Essential Modulator (NEMO) Gene Rearrangement in Korean Patients with Incontinentia Pigmenti | Semantic Scholar
![Incontinentia Pigmenti Associated with Aplasia Cutis Congenita in a Newborn Male with Klinefelter Syndrome: Is the Severity of Neurological Involvement Linked to Skin Manifestations? | Dermatology and Therapy Incontinentia Pigmenti Associated with Aplasia Cutis Congenita in a Newborn Male with Klinefelter Syndrome: Is the Severity of Neurological Involvement Linked to Skin Manifestations? | Dermatology and Therapy](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs13555-019-00336-z/MediaObjects/13555_2019_336_Fig3_HTML.jpg)