Arch Dermatol. 1976 Apr;112(4):535-42.

Incontinentia pigmenti. A world statistical analysis.

Abstract

Incontinentia pigmenti (Bloch-Sulzberger syndrome) is an uncommon genodermatosis that usually affects female infants. I reviewed 464 references from the world literature and found 653 apparently valid reports of patients with incontinentia pigmenti. Skin manifestations were found to be somewhat more common than previously reported, and systemic manifestations were found in 79.8% of the patients.

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[Incontinentia pigmenti (Bloch-Sulzberger syndrome)]. [Ned Tijdschr Geneeskd. 1984]
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Review Incontinentia pigmenti: a review.
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Cited by 21 PubMed Central articles

A Female Child with Skin Lesions and Seizures: Case report of Incontinentia Pigmenti. [Sultan Qaboos Univ Med J. 2009]
A Female Child with Skin Lesions and Seizures: Case report of Incontinentia Pigmenti.
Al-Zuhaibi S, Ganesh A, Al-Waili A, Al-Azri F, Javad H, Al-Futaisi A. Sultan Qaboos Univ Med J. 2009 Aug; 9(2):157-61. Epub 2009 Jun 30.
A case of incontinentia pigmenti associated with multiorgan abnormalities. [Ann Dermatol. 2009]
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Chung WK, Lee DW, Chang SE, Lee MW, Choi JH, Moon KC. Ann Dermatol. 2009 Feb; 21(1):56-9. Epub 2009 Feb 28.
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Incontinentia pigmenti presenting as hypodontia in a 3-year-old girl: a case report.
Kitakawa D, Fontes PC, Magalhães FA, Almeida JD, Cabral LA. J Med Case Rep. 2009 Nov 10; 3:116. Epub 2009 Nov 10.

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Incontinentia pigmenti. A world statistical analysis.

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Cited by 21 PubMed Central articles

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