Deletion within SMAD4 Gene Cause JPS Resulting in Total Abdominal Colectomy with Ileorectal Anastomosis

Mohammed AlBalwi, Abdullah AlZaben, Ibrahim AlAbdulkareem, Mohammed Afzal, Saud AlJadaan

Abstract: Juvenile polyposis syndrome (JPS) is an autosomal dominant disorder characterised by developed frequent benign gastrointestinal polyps from normal tissue that may transformed to malignancy. Here, we describe a patient with frequent bloody mucous diarrhea associated with lower abdominal pain and multiple variable sized polyps all over different segments of the colon. Molecular DNA sequencing revealed presence of a de nova heterozygous c.1245_1248CAGA mutation that located within the highly conserved MH2 domain of the SMAD4 gene. Familial molecular analysis showed that both parents are not carrier for any mutation. Therefore, such molecular study is important in confirming the diagnosis of JPS and identifying patient who barbering SMAD4 mutation and at high risk in developing malignancy. Thus, appropriate surveillance management care may provide

Keywords: SMAD4, juvenile polyposis syndrome, BMPR1A, autosomal

How to Cite?: Mohammed AlBalwi, Abdullah AlZaben, Ibrahim AlAbdulkareem, Mohammed Afzal, Saud AlJadaan, "Deletion within SMAD4 Gene Cause JPS Resulting in Total Abdominal Colectomy with Ileorectal Anastomosis", Volume 4 Issue 8, August 2015, International Journal of Science and Research (IJSR), Pages: 1955-1957, https://www.ijsr.net/getabstract.php?paperid=SUB157530, DOI: https://dx.doi.org/10.21275/SUB157530