Cri-Du-Chat Syndrome – A Rare Case Report

被引:0
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作者
Balaji Dhanasekaran
Rajasekaran Srinivasan
Priya Kanagamuthu
Prabakaran Somu
Namasivaya Navin R.B.
K. Gowthame
Sarath Kumar
C. Ramya Shree
S.R. Karthika
Greeshma U. Gopan
机构
[1] Chettinad Hospital and Research Institute,Dept. of ENT
关键词
Criduchat syndrome; Hearing loss; External auditory canal stenosis; Bera;
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摘要
The Cri-du-chat Syndrome (CdCs) is a rare genetic syndrome first described by Jerome Lejeune in 1963, characterized mainly by the high pitched cat like cry. The prevalence of CdCs was varied in between 1:15,000 to 1:50,000 in live birth and more common in female gender with a ratio of 4:3 [1, 2] .The condition may be accompanied by developmental and cognitive delays, poor spatial awareness, impaired ambulation, and poor sensori-motor skills. Other associated problems described include cardiovascular, renal, gastrointestinal, neurological abnormalities, preauricular tags, syndactyly, hypospadias, and cryptorchidism.1 Recent literatures show that autistic behaviours are common in various genetic disorders [3].Fatigue level of children with cri du chat syndrome was associated with the expression of autistic features [4].
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页码:3993 / 3998
页数:5
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