Literature DB >> 950303

[Ito's syndrome (incontinentia pigmenti achromians)].

R Happle, J Krenz, R Pfeiffer.   

Abstract

Ito's syndrome is a distinct entity characterized by bilateral systematized linear depigmentations denominated by Ito as "incontinentia pigmentiachromians". The syndrome includes a variety of anomalies predominantly affecting the central nervous system, the eyes, and the muscular-skeletal-system. The patient described in this paper was a 26 year old man suffering from a sever scoliosis. This anomaly had not been mentioned in previous case reports.

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Year:  1976        PMID: 950303

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  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.  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

3.  Hypomelanosis of Ito presenting with pediatric orthopedic issues: a case report.

Authors:  Malene Trägårdh; Christine Rohr Thomsen; Rikke Thorninger; Bjarne Møller-Madsen
Journal:  J Med Case Rep       Date:  2014-05-19
  3 in total

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