Literature DB >> 944355

[Hypomelanosis cutis ITO (author's transl)].

R A Pfeiffer, R Happle, G Stupperich.   

Abstract

Report on a 9 year old girl exhibiting the typical features of Ito's syndrome: systematized bilateral depigmented nevus associated with various nonspecific dysplasias. The pathogenesis is not known. The syndrome geems to be transmitted by an irregularly dominant gene.

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Mesh：

Year:  1976        PMID： 944355

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN： 0300-8630            Impact factor:   1.349


  4 in total

1.  Encephalitis in two members of a family with incontinentia pigmenti (Bloch-Sulzberger syndrome). The possible role of inflammation in the pathogenesis of CNS involvement.

Authors:  H Siemes; H Schneider; D Dening; F Hanefeld
Journal:  Eur J Pediatr       Date:  1978-09-08       Impact factor: 3.183

2.  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

3.  Hypomelanosis of ito is frequently associated with autism.

Authors:  Michele Zappella
Journal:  Eur Child Adolesc Psychiatry       Date:  1992-07       Impact factor: 4.785

4.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  4 in total

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