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pubmed-article:1890574pubmed:abstractTextIncontinentia pigmenti achromians is a multisystem hereditary disorder characterized specifically by a whorled or streaked cutaneous hypopigmentation and frequently characterized by numerous neurologic, musculoskeletal, and ocular abnormalities. We present a patient with incontinentia pigmenti achromians in whom the ocular abnormalities included the commonly reported exotropia, myopia, small optic nerve, and hypopigmentation of the fundus, as well as rarely reported corneal asymmetry, pannus, and atropic irides with irregular pupillary margins. The patient also had a cataract in the right eye and a retinal detachment in the left eye.lld:pubmed
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pubmed-article:1890574pubmed:authorpubmed-author:MartinTTlld:pubmed
pubmed-article:1890574pubmed:authorpubmed-author:ZanolliM DMDlld:pubmed
pubmed-article:1890574pubmed:authorpubmed-author:WeaverR GRGJrlld:pubmed
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pubmed-article:1890574pubmed:volume28lld:pubmed
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pubmed-article:1890574pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:1890574pubmed:articleTitleThe ocular changes of incontinentia pigmenti achromians (hypomelanosis of Ito).lld:pubmed
pubmed-article:1890574pubmed:affiliationDepartment of Ophthalmology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27103.lld:pubmed
pubmed-article:1890574pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1890574pubmed:publicationTypeCase Reportslld:pubmed
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