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- W4213292780 abstract "Craniometaphyseal dysplasia (CMD) is an extremely rare genetic disease marked by progressive thickening of the craniofacial bones and aberrant development of the metaphyses in long bones. As a result of diffuse hyperostosis of the skull base, neurological symptoms associated with cranial nerve compression, such as reduced vision, cranial nerve palsy, and deafness can occur. Craniofacial abnormalities are prominent and include hypertelorism, frontonasal bossing, a broad nasal root, prognathic mandible, and defective dentition [[1]]. In this paper, the authors report a case of CMD associated with facial dysmorphism and mild hearing loss in a 4-year-old girl. The clinical aspects, pathogenesis, and management of CMD will be reviewed." @default.
- W4213292780 created "2022-02-24" @default.
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- W4213292780 date "2013-01-01" @default.
- W4213292780 modified "2023-10-16" @default.
- W4213292780 title "Craniometaphyseal Dysplasia" @default.
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- W4213292780 doi "https://doi.org/10.5999/aps.2013.40.2.157" @default.
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