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Abstract
COJ Technical & Scientific Research
Cornelia de Lange Syndrome: A Rare Disease
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Open or CloseKarabi Biswas* and Sankar Narayan S
Microbiology and Virology Section, University of Kalyani, India
*Corresponding author: Karabi Biswas, Microbiology and Virology Section,Department of Botany, Kalyani-741235, West Bengal, India
Submission: September 7, 2020; Published: November 24, 2020
Abstract
Cornelia de Lange syndrome is a rare, genetic sickness that clearly impacts each physical device and ends in an array of bodily and cognitive deficits. Most of them with this syndrome are identified at the time of birth. SMC1A, SMC3, HDAC8 and RAD21 genes are responsible for this disease. Cornelia de Lange syndrome has complex manifestations, that can variety from moderate to severe. The analysis of Cornelia de Lange syndrome is primarily based totally on medical findings of its function symptoms and symptoms and signs as evaluated via way of means of a physician.Treatment for Cornelia de Lange syndrome is lifelong and may be complex, with variations relying on every precise case.
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