“…Those authors recommend sonography every 5 years for all patients with TS and annually if an abnormality is detected. The polycystic form of renal involvement, described in the article by Wheeler et al, 1 frequently has its presentation in infancy or early childhood and can usually be managed conservatively. Another, less common form, is multiple hamartomatous changes with cysts and small angiomyolipomas; this form may be associated with a higher risk of renal impairment and has been postulated to have genetic implications of a ''double hit.''…”