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Updated: Nov 21, 2025

Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium
Published on: September 1, 2015
Turner syndrome and autosomal dominant polycystic kidney disease
Rachel Styer1, Matthew Stephen2, Faris Hashim3
1Department of Pediatrics, Texas A&M Health Science Center, Baylor Scott & White McLane Children Medical Center, Temple, Texas.
Abstract:
Turner syndrome is a chromosomal disorder that involves multiple organ systems and is typically associated with short stature. A multidisciplinary approach with regular screening and surveillance is key to managing this condition's multiple comorbidities. We present a case of a young girl with Turner syndrome and associated short stature on growth hormone treatment who presented with cystic renal disease found to be autosomal dominant kidney disease. We propose reevaluation of renal screening guidelines in this population due to the potential association of growth hormone and cyst proliferation.
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