Literature DB >> 24260612

A 14-year-old girl with an unusual combination of incontinentia pigmenti and conversion disorder.

Yan Wang1, Yihui Chen, Qiaoshu Wang, Guodong Wang, Chunni Guo, Feng Wang, Xiaolei Deng, Weizhen Wang.   

Abstract

Incontinentia pigmenti is a rare X-linked neurological-skin genetic disease. Some studies have shown that about 30~40% of patients with IP have varying symptoms of eye/central nervous system which are the major causes of disability. Conversion disorder is one of the most common mental diseases in children and may exhibit the single or multiple neurological symptoms. In this paper, we will report a child with new and rare incontinentia pigmenti accompanied by conversion disorder and explore the relationship of this rare combination.

Entities:  

Keywords:  Incontinentia pigmenti; X chromosome-linked dominant genetic disease; central nervous system; conversion disorder

Year:  2013        PMID： 24260612      PMCID： PMC3832343     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN： 1940-5901


  9 in total

1.  Conversion disorder after surgery in a brain tumour patient.

Authors:  Kathleen Joy Khu; Sherese Ali; Mark Bernstein
Journal:  Can J Neurol Sci       Date:  2010-03       Impact factor: 2.104

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Journal:  Br J Psychiatry       Date:  1995-01       Impact factor: 9.319

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Authors:  O Devinsky; S Mesad; K Alper
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2001       Impact factor: 2.198

Review 5.  Incontinentia pigmenti: a review and update on the molecular basis of pathophysiology.

Authors:  Alexander L Berlin; Amy S Paller; Lawrence S Chan
Journal:  J Am Acad Dermatol       Date:  2002-08       Impact factor: 11.527

6.  Multiple sclerosis and hysteria. Lessons learned from their association.

Authors:  L R Caplan; T Nadelson
Journal:  JAMA       Date:  1980-06-20       Impact factor: 56.272

Review 7.  Neurological findings in incontinentia pigmenti; a review.

Authors:  Marije E C Meuwissen; Grazia M S Mancini
Journal:  Eur J Med Genet       Date:  2012-05-04       Impact factor: 2.708

8.  Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes.

Authors:  S Aradhya; T Bardaro; P Galgóczy; T Yamagata; T Esposito; H Patlan; A Ciccodicola; A Munnich; S Kenwrick; M Platzer; M D'Urso; D L Nelson
Journal:  Hum Mol Genet       Date:  2001-10-15       Impact factor: 6.150

9.  Two cases of misinterpretation of molecular results in incontinentia pigmenti, and a PCR-based method to discriminate NEMO/IKKgamma dene deletion.

Authors:  Tiziana Bardaro; Geppino Falco; Angela Sparago; Vincenzo Mercadante; Esther Gean Molins; Enrico Tarantino; Matilde Valeria Ursini; Michele D'Urso
Journal:  Hum Mutat       Date:  2003-01       Impact factor: 4.878
  9 in total

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