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Hearing Loss in Syndromic Craniosynostoses: Introduction and Consideration of Mechanisms
PURPOSE: There are a number of craniosynostosis syndromes with hearing loss—including Muenke, Apert, Pfeiffer, Crouzon, Beare-Stevenson, Crouzon with acanthosis nigricans, and Jackson-Weiss syndromes—that result from mutations in the fibroblast growth factor receptor (FGFR) genes. Studies of FGFRs a...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4131981/ https://ncbi.nlm.nih.gov/pubmed/24686979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1044/2014_AJA-13-0036 |
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