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ISSN Print: 2394-7500, ISSN Online: 2394-5869, CODEN: IJARPF

Impact Factor: RJIF 8.4

International Journal of Applied Research

Vol. 2, Issue 3, Part B (2016)

Edward syndrome with hepatoblastoma: A case report

Author(s)
Dr. Anshuman Singh, Dr. Sharad Agarkhedkar, Dr. Kumar Gaurav
Abstract
Edward syndrome is a condition of developmental delay and dysmorphology caused due to trisomy 18 disrupting the normal course development, causing the characteristic features of Edward syndrome. The main characteristics of Edward syndrome are: intra- extra uterine growth retardation, mental retardation with typical facial dysmorphism, microcephaly and mid line defects. When only some of the body’s cells have an extra copy of chromosome 18, is called mosaic Edward syndrome and is a very rare form. Here we describe a female baby with mosaic trisomy 18, who had a majority of the main phenotypic feature.
Pages: 75-77  |  654 Views  15 Downloads
How to cite this article:
Dr. Anshuman Singh, Dr. Sharad Agarkhedkar, Dr. Kumar Gaurav. Edward syndrome with hepatoblastoma: A case report. Int J Appl Res 2016;2(3):75-77.
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International Journal of Applied Research