Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis

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Name:
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Description:
A rare contiguous gene syndrome involving a partial deletion of chromosome 16 and characterized by early-onset and severe polycystic kidney disease with various manifestations of tuberous sclerosis (multiple angiomyolipomas, lymphangioleiomyomatosis and periventricular calcifications of the central nervous system).
ORPHAcode:
88924
Synonyms:
PKDTS
TSC2/PKD1 contiguous gene syndrome
Tuberous sclerosis/polycystic kidney disease contiguous gene syndrome
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14