Incontinentia pigmenti in a father and daughter

Author:

Rashidghamat E.1,Hsu C.K.12,Nanda A.3,Liu L.4,Al-Ajmi H.3,McGrath J.A.1

Affiliation:

1. St. John's Institute of Dermatology; King's College London; London U.K

2. Department of Dermatology; National Cheng Kung University Hospital; College of Medicine; National Cheng Kung University; Tainan Taiwan

3. As'ad Al-Hamad Dermatology Center; Al-Sabah Hospital; Kuwait

4. Viapath, St Thomas's Hospital; London U.K

Funder

National Institute for Health Research

Guy's and St Thomas' NHS Foundation Trust

King’s College London

Publisher

Wiley

Subject

Dermatology

Reference6 articles.

1. Genomic rearrangement in NEMO impairs NF-kappa-B activation and is a cause of incontinentia pigmenti;Smahi;The International Incontinentia Pigmenti Consortium. Nature,2000

2. Incontinentia pigmenti: report on data from 2000 to 2013;Fusco;Orphanet J Rare Dis,2014

3. Improved molecular diagnosis of the common recurrent intragenic deletion mutation in IKBKG in a Filipino family with incontinentia pigmenti;Guevara;Australas J Dermatol,2016

4. Incontinentia pigmenti in a father and his daughter;Sommer;Am J Med Genet,1984

5. Incontinentia pigmenti: transmission from father to daughter;Emery;J Am Acad Dermatol,1993

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1. Variable clinical consequences of mosaicism for c.1167dupC in IKBKG in male and female patients with incontinentia pigmenti and related phenotypes;Clinical and Experimental Dermatology;2023-10-25

2. Generalized and Localized Genetic Hyperpigmentation;Atlas of Pigmentary Skin Disorders;2023

3. Incontinentia pigmenti in a male infant and a proposed diagnostic algorithm;Clinical and Experimental Dermatology;2022-04-18

4. Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male;International Journal of Molecular Sciences;2022-01-21

5. INCONTINENTIA PIGMENTI;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30

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