| Literature DB >> 24683199 |
Nur Farrah Dila Ismail1, Nik Mohd Ariff Nik Abdul Malik, Jafar Mohseni, Abdulqawee Mahyoob Rani, Fatemeh Hayati, Abdul Razak Salmi, Mohd Yusof Narazah, Z A M H Zabidi-Hussin, Abdul Rashid Silawati, Wee Teik Keng, Lock Hock Ngu, Teguh Haryo Sasongko.
Abstract
Tuberous sclerosis complex is an autosomal dominant neurocutaneous disorder affecting multiple organs. Tuberous sclerosis complex is caused by mutation in either one of the two disease-causing genes, TSC1 or TSC2, encoding for hamartin and tuberin, respectively. TSC2/PKD1 contiguous gene deletion syndrome is a very rare condition due to deletion involving both TSC2 and PKD1 genes. Tuberous sclerosis complex cannot be easily diagnosed since there is no pathognomonic feature, although there are consensus diagnostic criteria for that. Mutation analysis is useful and plays important roles. We report here two novel gross deletions of TSC2 gene in Malay patients with tuberous sclerosis complex and TSC2/PKD1 contiguous gene deletion syndrome, respectively.Entities:
Keywords: PKDTS; TSC2; TSC2/PKD1 Contiguous gene deletion syndrome; Tuberous sclerosis complex
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Year: 2014 PMID: 24683199 DOI: 10.1093/jjco/hyu024
Source DB: PubMed Journal: Jpn J Clin Oncol ISSN: 0368-2811 Impact factor: 3.019