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- W2396212575 abstract "Treacher Collins syndrome is seen once in 10.000 births. Inheritance is autosomal dominant with variable expressivity. The most prominent symptoms are antimongoloid slant of the eyelids, hypo- or even aplasia of the zygomata, very hypoplastic mandible with receding chin, deformed ear lobes and conductive hearing loss. With two to three operations a considerable improvement can be achieved. The correction of the eyelids is often the most difficult problem." @default.
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- W2396212575 date "1999-06-01" @default.
- W2396212575 modified "2023-09-25" @default.
- W2396212575 title "[Syndromes 11. Treacher collins syndrome]." @default.
- W2396212575 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11930479" @default.
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