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pubmed-article:1388933pubmed:abstractTextIn this report we describe an 8-year-old boy of Algerian origin with profound sensorineural deafness and skin pigmentation anomalies consistent with the diagnosis of hypomelanosis of Ito. On the basis of this observation the etiologic heterogeneity of this condition is discussed.lld:pubmed
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pubmed-article:1388933pubmed:authorpubmed-author:Van Den...lld:pubmed
pubmed-article:1388933pubmed:authorpubmed-author:DereymaekerA...lld:pubmed
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pubmed-article:1388933pubmed:pagination149-51lld:pubmed
pubmed-article:1388933pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:1388933pubmed:year1992lld:pubmed
pubmed-article:1388933pubmed:articleTitleHypomelanosis of Ito and severe sensorineural deafness.lld:pubmed
pubmed-article:1388933pubmed:affiliationCentre for Human Genetics, University of Leuven, Belgium.lld:pubmed
pubmed-article:1388933pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1388933pubmed:publicationTypeCase Reportslld:pubmed