| Oculodentodigital dysplasia syndrome. Report of four cases. | |
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MedLine Citation:
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PMID: 197779 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Four cases of oculodentodigital dysplasia are reported. Three cases are from the same family, father and two daughers. These three cases have the characteristics typical of this disorder: narrow nose, hypoplastic alae nasi, microphthalmia, defects of the teeth, syndactylyl of the IV and V fingers, and skeletal anomalies. The fourth case differs from the earlier reported cases; he has all the typical findings of oculodentodigital dysplasia but in addition he shows features not previously reported, namely exceptionally poor vision, mental retardation, monilethrix and pili annuli changes of the hair. |
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Authors:
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C J Thodén; S Ryöppy; P Kuitunen |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Acta paediatrica Scandinavica Volume: 66 ISSN: 0001-656X ISO Abbreviation: Acta Paediatr Scand Publication Date: 1977 Sep |
Date Detail:
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Created Date: 1977-10-28 Completed Date: 1977-10-28 Revised Date: 2009-11-11 |
Medline Journal Info:
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Nlm Unique ID: 0000211 Medline TA: Acta Paediatr Scand Country: SWEDEN |
Other Details:
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Languages: eng Pagination: 635-8 Citation Subset: IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple Adult Amelogenesis Imperfecta Child, Preschool Dental Enamel Hypoplasia Eye Abnormalities* Female Humans Male Mental Retardation Syndactyly* Syndrome Tooth Abnormalities* Vision Disorders / congenital |
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