Fetal and Postnatal Magnetic Resonance Imaging of Unilateral Cystic Renal Dysplasia in a Neonate with Tuberous Sclerosis

Tuberous sclerosis (TS) is an autosomal dominant condition associated with mutations in the TSC1 and/or TSC2 genes. Clinical manifestations are multisystemic, and they often include lesions in the brain, skin, heart, kidneys, and bones. TSC2 gene mutations can be seen concomitantly with autosomal do...

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Main Authors: Vineet Tyagi (Author), Eran Bornstein (Author), Robert Schacht (Author), Shailee Lala (Author), Sarah Milla (Author)
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出版: Elsevier, 2016-10-01T00:00:00Z.
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