Literature DB >> 28711407

Severe neuroimaging anomalies are usually associated with random X inactivation in leucocytes circulating DNA in X-linked dominant Incontinentia Pigmenti.

Volodia Dangouloff-Ros1, Smail Hadj-Rabia2, Judite Oliveira Santos3, Elodie Bal3, Isabelle Desguerre4, Manoelle Kossorotoff5, Isabelle An6, Asma Smahi3, Christine Bodemer2, Arnold Munnich7, Julie Steffann7, Nathalie Boddaert8.   

Abstract

Incontinentia Pigmenti (IP) is a skin disorder with neurological impairment in 30% of cases. The most common disease causing mutation is a deletion of exons 4-10 of the IKBKG gene, located on chromosome Xq28, with skewed X-chromosome inactivation in females, but few cases of random X-inactivation have been reported. We have correlated brain anomalies with X-chromosome inactivation status determined on leucocytes circulating DNA. We reviewed MRI of 18 girls with genetically proven IP. We found three patterns of MRI, normal MRI (n=5), mild white matter abnormalities with cortical and corpus callosum atrophy (n=6), and severe cortical abnormalities suggesting a vascular disease (n=7). Most patients with severe abnormalities had random X-inactivation (6/7,86%), while 80% (4/5) of patients with normal MRI and 100% (6/6) of patients with mild white matter abnormalities had skewed inactivation. These results suggest that skewed chromosome X-inactivation may protect brain from damage, while in case of random inactivation, expression of the mutated IKBKG gene may lead to severe brain lesions.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Brain; IKBKG protein, human; Incontinentia Pigmenti; Magnetic Resonance Imaging; X chromosome inactivation

Mesh:

Substances:

Year:  2017        PMID: 28711407     DOI: 10.1016/j.ymgme.2017.07.001

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  3 in total

1.  Unilateral Cerebral Atrophy: Severe Neuroimaging Feature of Incontinentia Pigmenti without Acute Encephalopathic State.

Authors:  Debopam Samanta
Journal:  J Pediatr Neurosci       Date:  2018 Apr-Jun

2.  Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation.

Authors:  Snežana Minić; Dušan Trpinac; Ivana Novaković; Nataša Cerovac; Danijela Dobrosavljević Vukojević; Jérémie Rosain
Journal:  Diagnostics (Basel)       Date:  2022-07-14

Review 3.  Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology.

Authors:  Kang Nien How; Hazel Jing Yi Leong; Zacharias Aloysius Dwi Pramono; Kin Fon Leong; Zee Wei Lai; Wei Hsum Yap
Journal:  Front Pediatr       Date:  2022-09-06       Impact factor: 3.569

  3 in total

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