Literature DB >> 2409793

Incontinentia pigmenti. A longitudinal study.

J E O'Brien, M Feingold.   

Abstract

We describe 15 patients with incontinentia pigmenti whom we have followed up from two to 11 years. This longitudinal approach allowed us to observe the course of the skin lesions and developmental progress of these children. We found that in contrast to what has been previously reported in most of the literature, the bullous and verrucous lesions do not always resolve during the first or second year of life and may recur throughout childhood. Although most patients with incontinentia pigmenti are of normal intelligence, those with neonatal seizures have a poor prognosis for normal development.

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Year:  1985        PMID: 2409793     DOI: 10.1001/archpedi.1985.02140090073033

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  3 in total

Review 1.  Incontinentia pigmenti (Bloch-Sulzberger syndrome): report of a case and review of the Indian literature.

Authors:  S N Tomaraei; R P Bajwa; P Dhiman; R K Marwaha
Journal:  Indian J Pediatr       Date:  1995 Jan-Feb       Impact factor: 1.967

Review 2.  Incontinentia pigmenti (Bloch-Sulzberger syndrome).

Authors:  S J Landy; D Donnai
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

3.  A Female Child with Skin Lesions and Seizures: Case report of Incontinentia Pigmenti.

Authors:  Sana Al-Zuhaibi; Anuradha Ganesh; Ahmed Al-Waili; Faisal Al-Azri; Hashim Javad; Amna Al-Futaisi
Journal:  Sultan Qaboos Univ Med J       Date:  2009-06-30
  3 in total

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