WSI23-38-Case-32

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Revision as of 08:40, May 9, 2023 by Aja51 (talk | contribs)
WSI23-38-Case-32
7 year old male with h/o tuberous sclerosis and polycystic kidney disease
Papillary renal cell, multiple type II and type I angiolipoma, PCKD (contiguous gene detection syndrome)
April 1, 2023 12:00:00 PM







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