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Article

Tuberous sclerosis complex with autosomal dominant polycystic kidney disease: a rare duo.

BMJ case reports - 17 Dec 2014

Rijal Jharendra P, Dhakal Prajwal, Giri Smith, Dahal Khagendra V

Abstract excerpt

Tuberous sclerosis complex (TSC) is an autosomal dominant condition characterised by the presence of multiple hamartomas in various organ systems in the body. The kidneys are affected in 80% of patients, usually in the form of renal angiomyolipomas, renal cysts or renal cell carcinoma. Although extremely rare, TSC and autosomal dominant polycystic kidney disease (ADPKD) can co-exist in the same patient as a...

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Share to Chromosomes, Human, Pair 16
Share to Kidney
Share to Polycystic Kidney, Autosomal Dominant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Renal Insufficiency

Share to TRPP Cation Channels

Share to Tuberous Sclerosis

Share to Tuberous Sclerosis Complex 2 Protein

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Source

Open in PubMed Open full text

Identifiers

PMID: 25519866
DOI: 10.1136/bcr-2014-207471
PMCID: PMC4275747

Genes

TSC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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