Postzygotic mosaicism and incontinentia pigmenti in male patients: molecular diagnosis yield

Br J Dermatol. 2018 Apr;178(4):e261-e262. doi: 10.1111/bjd.16092. Epub 2018 Feb 6.

Authors

Z Alabdullatif¹, J Coulombe¹, J Steffann², C Bodemer¹, S Hadj-Rabia¹

Affiliations

¹ Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, INSERM U1163, Institut Imagine, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Paris, France.
² Department of Genetics, Université Paris Descartes - Sorbonne Paris Cité, INSERM U1163, Institut Imagine, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Paris, France.

PMID: 29077987
DOI: 10.1111/bjd.16092

No abstract available

Publication types

Letter

MeSH terms

Apoptosis / genetics
Child, Preschool
Humans
I-kappa B Kinase / genetics*
Incontinentia Pigmenti / genetics*
Infant
Infant, Newborn
Male
Mosaicism*
Mutation / genetics

Substances

IKBKG protein, human
I-kappa B Kinase