五、治疗

五、治疗

无特殊治疗,预后多较好,对生存无大影响,对功能影响大小决定于畸形严重程度,必要时可进行整形手术。

参考文献

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[3]Monroe G R,Kappen I F,Stokman M F,et al.Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type Ⅱ(Mohr syndrome)[J].European Journal of Human Genetics,2016,24(12):1752-1760.

[4]Bouman A,Alders M,Oostra R J,et al.Oral-facial-digital syndrome type 1 in males:Congenital heart defects are included in its phenotypic spectrum[J].American Journal of Medical Genetics Part A,2017,173(5):1383-1389.

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(王翔 王文梅)