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Journal Article
Actas Dermo-Sifiliográficas (English Edition), ISSN 1578-2190, 05/2019, Volume 110, Issue 4, pp. 273 - 278
Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. It is an X-linked dominant disorder caused by mutations in the gene on... 
Clínica | Clinical features | Incontinentia pigmenti | Treatment | Diagnóstico | Tratamiento | Diagnosis | IKBKG/NEMO | Incontinencia pigmenti
Journal Article
Actas Dermo-Sifiliograficas, ISSN 0001-7310, 2019
Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. It is an X-linked dominant disorder caused by mutations in the... 
Clinical features | Incontinentia pigmenti | Treatment | Diagnosis | IKBKG/NEMO
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2019, Volume 179, Issue 8, pp. 1415 - 1419
Incontinentia Pigmenti (IP; MIM 308300) is an X‐linked dominant genodermatosis caused by pathogenic variant in IKBKG . The phenotype in adults is poorly... 
phenotype | Incontinentia Pigmenti | ectodermal dysplasia | IKBKG | adult | BLOCH-SULZBERGER | ACTIVATION | GENETICS & HEREDITY | Dysplasia | Adults | Skin | Market surveys | Cataracts | Dentures | Jaw | Phenotypes | Nails | Retina | Cognition | Polls & surveys | Genodermatosis | Intolerance | Surgery | Diagnosis | Microphthalmia
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 09/2016, Volume 33, Issue 5, pp. e280 - e281
Late recurrences of first‐stage inflammatory vesiculobullous lesions of incontinentia pigmenti ( IP ) are uncommon but have been reported to occur in the... 
PEDIATRICS | DERMATOLOGY | Incontinentia Pigmenti - diagnosis | Coxsackievirus Infections - diagnosis | Humans | Infant | Male | Coxsackievirus Infections - complications | Incontinentia Pigmenti - virology | Coxsackievirus infections
Journal Article
Kathmandu University Medical Journal, ISSN 1812-2027, 01/2013, Volume 11, Issue 41, pp. 91 - 93
Journal Article
Molecular Cell, ISSN 1097-2765, 2000, Volume 5, Issue 6, pp. 981 - 992
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2018, Volume 176, Issue 11, pp. 2318 - 2324
Incontinentia Pigmenti (IP) is an X‐linked rare genodermatosis caused by mutations in the IKBKG gene, which is essential to NF‐κB pathway activation and thus... 
genodermatosis | incontinentia pigmenti | IKBKG | NEMO | REARRANGEMENT | GENETIC-BASIS | ALLELES | GENETICS & HEREDITY | MUTATIONS | EXPRESSION | Medicine, Experimental | Medical research | Genodermatosis | Incontinentia Pigmenti | IKBKG gene | Cell survival | Clonal deletion
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 03/2019, Volume 81, Issue 5, pp. 1142 - 1149
Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis that affects multiple systems with highly variable phenotypic expressivity. Although... 
Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 8/2013, Volume 172, Issue 8, pp. 1137 - 1138
Incontinentia pigmenti (IP) is an uncommon X-linked dominant genodermatosis. It affects predominantly females and is lethal in utero in male fetuses. We herein... 
Medicine & Public Health | Pediatrics | Incontinentia pigmenti | PEDIATRICS | Incontinentia Pigmenti - genetics | Humans | Incontinentia Pigmenti - pathology | Genetic Diseases, X-Linked - pathology | Female | Infant | Infant, Newborn | Skin - pathology | Index Medicus
Journal Article
Journal Article