全部文献期刊会议图书|学者科研项目
中外文文献  中文文献  外文文献
作者:Dhivya Ashok Kumar , Amar Agarwal
来源:[J].Indian Journal of Ophthalmology(IF 1.019), 2017, Vol.65 (9), pp.884-886
摘要:An upper lid eccrine hidrocystoma presenting as early childhood progressive ptosis is very rare. We present a 9-year-old female child with droopy right upper lid since birth and progressive increase in symptoms. She had right upper lid ptosis (marginal reflex distance 1 of −1 ...
作者:Dhivya Kumar , Amar Agarwal
来源:[J].Indian Journal of Ophthalmology(IF 1.019), 2017, Vol.65 (9), pp.884-886
摘要:An upper lid eccrine hidrocystoma presenting as early childhood progressive ptosis is very rare. We present a 9-year-old female child with droopy right upper lid since birth and progressive increase in symptoms. She had right upper lid ptosis (marginal reflex distance 1 of −1 ...
作者:Kumar Dhivya Ashok , Agarwal Amar
来源:[J].Indian journal of ophthalmology, 2017, Vol.65 (9), pp.884-886
摘要:An upper lid eccrine hidrocystoma presenting as early childhood progressive ptosis is very rare. We present a 9-year-old female child with droopy right upper lid since birth and progressive increase in symptoms. She had right upper lid ptosis (marginal reflex distance 1 of -1 ...
作者:Małgorzata Dorobek , Dagmara Kabzińska
来源:[J].European Journal of Paediatric Neurology(IF 1.982), 2004, Vol.8 (6), pp.313-316
摘要:... In this report, we describe a case of severe, infantile onset FSHD in a patient with asymmetric progressive ptosis and early hyperlordosis. DNA analysis revealed a very short 4q35 allele of 8.6 kb and a somatic mosaicism for the 4q35 deletion detected in a subclinically affec...
作者:Victor Maurice , Hayes Robert , Adams Raymond D.
来源:[J].The New England Journal of Medicine(IF 51.658), 1962, Vol.267 (25), pp.1267-1272
摘要:... Taylor 1 called attention to an unusual familial form of dysphagia with ptosis of the eyelids. These symptoms were slowly progressive, leading eventually to death by starvation. Taylor contended, after the customary search of the medical literature, that the disease had not p...
作者:Y.H.J. Chai
来源:[J].Neuromuscular Disorders(IF 3.464), 2014, Vol.24 (9-10), pp.796-796
摘要:Oculopharyngeal muscular dystrophy (OPMD) is a late-onset autosomal dominant disorder presenting with progressive ptosis and dysphagia, due to GCN trinucleotide repeat in PABPN1 . OPMD is rarely seen in the Far East and genetically confirmed case has not been reported in Sin...

我们正在为您处理中,这可能需要一些时间,请稍等。

资源合作:cnki.scholar@cnki.net, +86-10-82896619   意见反馈:scholar@cnki.net

×