ISSN: 2332-0877

Journal of Infectious Diseases & Therapy
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  • Short Communication   
  • J Infect Dis Ther 2019, Vol 7(1): 388
  • DOI: 10.4172/2332-0877.1000388

An Ultra-rare Hereditary Disease of 28–year Old Pregnant Patient withMalignant Alteration

Vuka Katic1*, Zoran Radovanovic1, Aleksandra Karadzic1, Goran Rankovic2, Ivan Nagorni1, Aleksandar Rankovic1 and Ivana Golubovic1
1Policlinic Human, Nis University, Serbia
2Faculty for Sports, Nis University, Serbia
*Corresponding Author : Vuka Katic, Policlinic Human, Nis University, Serbia, Tel: 0038118533190, Email: vuka.katic@gmail.com

Received Date: Nov 23, 2018 / Accepted Date: Dec 06, 2018 / Published Date: Dec 12, 2018

Abstract

Familial adenomatous polyposis (FAP) is an autosomal dominant disorder characterized by the development of hundreds to thousands of colorectal adenomatous polyps and the inevitable occurrence of colorectal carcinoma, if the colon is not removed. In a 28-year old patient, following diagnostic criteria, have been established more than 500 colorectal adenomas and family history of FAP.

Keywords: Colorectal; Carcinoma; Adenocarcinoma; Rectal carcinoma; Antibodies

Citation: Katic V, Radovanovi Z, Karadzic A, Rankovic G, Nagorni I, et al. (2018) An Ultra-rare Hereditary Disease of 28–year Old Pregnant Patient with Malignant Alteration. J Infect Dis Ther 7:388. Doi: 10.4172/2332-0877.1000388

Copyright: © 2018 Katic V, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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