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pubmed-article:950303pubmed:issue6lld:pubmed
pubmed-article:950303pubmed:dateCreated1976-10-2lld:pubmed
pubmed-article:950303pubmed:abstractTextIto'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.lld:pubmed
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pubmed-article:950303pubmed:issn0017-8470lld:pubmed
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pubmed-article:950303pubmed:authorpubmed-author:KrenzJJlld:pubmed
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pubmed-article:950303pubmed:volume27lld:pubmed
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pubmed-article:950303pubmed:pagination286-90lld:pubmed
pubmed-article:950303pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:950303pubmed:year1976lld:pubmed
pubmed-article:950303pubmed:articleTitle[Ito's syndrome (incontinentia pigmenti achromians)].lld:pubmed
pubmed-article:950303pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:950303pubmed:publicationTypeEnglish Abstractlld:pubmed
pubmed-article:950303pubmed:publicationTypeCase Reportslld:pubmed