| Waardenburg's syndrome: case reports in two Nigerians. | |
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MedLine Citation:
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PMID: 458527 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We saw two cases of Waardenburg's syndrome in Nigerian children. A 9-year-old girl had congenital deaf-mutism, high-arched palate, complete heterochromia iridis with pigment mottling in the posterior pole of the eye with the hypochromic iris, dyspigmented frontal scalp hair, a history of vitiligo, but with no dystopia canthorum. An 11-year-old boy had a harelip with cleft palate, heterochromia iridis, blonde fundus on the eye with blue iris, and dystopia canthorum. |
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Authors:
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S S Amoni; M B Abdurrahman |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Journal of pediatric ophthalmology and strabismus Volume: 16 ISSN: 0191-3913 ISO Abbreviation: J Pediatr Ophthalmol Strabismus Publication Date: 1979 May-Jun |
Date Detail:
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Created Date: 1979-09-25 Completed Date: 1979-09-25 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 7901143 Medline TA: J Pediatr Ophthalmol Strabismus Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 172-5 Citation Subset: IM |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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diagnosis* Child Cleft Lip / complications* Cleft Palate / complications* Deafness / complications Eye Color Female Humans Male Nigeria Pigmentation Disorders / complications* Waardenburg's Syndrome / complications, diagnosis* |
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