@article{Kankante_Misal_Mhaske_2018, title={Emanuel Syndrome: A Case Report}, volume={5}, url={https://vimshsj.edu.in/index.php/main/article/view/104}, abstractNote={<p>Emanuel Syndrome or Supernumerary derivative (22) syndrome is one of the rare genomic syndromes. It is characterised by severe mental retardation, microcephaly, failure to thrive, ear anomalies, pre-auricular tags or sinus, cleft palate or high arch palate, micrognathia, renal anomalies, congenital cardiac defects and genital abnormalities in males . In 99 percent of the cases, one of the parents is a balanced carrier of a translocation between chromosome 11 and chromosome 22. We report the first known case, a male neonate, of supernumerary derivative (22) syndrome<strong>.</strong></p>}, number={3}, journal={VIMS Health Science Journal }, author={Kankante, Dr. Santoshi and Misal, Dr. Ganesh and Mhaske, Dr. Sunil Natha}, year={2018}, month={Sep.}, pages={131–132} }