| Literature DB >> 26591174 |
Shyamashis Das, Bapi Lal Bala, Achintya Narayan Ray, Pasang Lahmu Sherpa, Rajiv Ranjan Kumar.
Abstract
Tuberous sclerosis complex (TSC) and autosomal dominant polycystic kidney disease (ADPKD) are two different genetic diseases. Although these two diseases are associated very rarely, the association is well recognized. This occurs due to a large deletion involving both PKD-1 and TSC-2 genes on chromosome 16. This is also known as TSC-2/PKD-1 contiguous gene syndrome. We report a 26-year-old female patient with TSC who presented with severe metabolic acidosis due to renal failure. She had palpable enlarged kidneys bilaterally. CT scan of abdomen revealed bilateral enlarged lobulated kidneys studded with multiple cysts which was consistent with the diagnosis of ADPKD.Entities:
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Year: 2015 PMID: 26591174
Source DB: PubMed Journal: J Assoc Physicians India ISSN: 0004-5772