Literature DB >> 1137418

Incontinentia pigmenti achromians.

A Griffiths, C Payne.   

Abstract

A patient with incontinentia pigmenti archromians, who was born to consanguineous parents, is described. This is the first reported case from Iran, to our knowledge. A number of features of this disease belong more properly to classical incontinentia pigmenti.

Entities:  

Mesh：

Year:  1975        PMID： 1137418

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN： 0003-987X


  3 in total

1.  Klinefelter's syndrome and incontinentia pigmenti Bloch-Sulzberger.

Authors:  J Kunze; U H Frenzel; E Hüttig
Journal:  Hum Genet       Date:  1977-02-11       Impact factor: 4.132

2.  Hypomelanosis of Itô: a neurocutaneous syndrome.

Authors:  T J David
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791

3.  Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report.

Authors:  Giovanni Ponti; Giovanni Pellacani; Aldo Tomasi; Antonio Percesepe; Carmelo Guarneri; Azzurra Guerra; Victor Desmond Mandel; Elif Kisla; Piril Cevikel; Claudia Neri; Cristina Menozzi; Stefania Seidenari
Journal:  J Med Case Rep       Date:  2014-10-09
  3 in total

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