A 10-year-old boy presents with severe abdominal pain and urinary urgency. He denies any dysuria, hematuria, frequency, meatal spotting, penile discharge, or incontinence. He has had no recent viral infections or fevers and he denies any history of perineal trauma. He has no significant medical or surgical past medical history. Three days earlier, he was seen at a local hospital with a 3-day history of increasing difficulty with voiding, including straining to void and incomplete bladder emptying. A bladder scan revealed a full bladder after he voided. Therefore, an 8-French catheter was placed and he was told to return in 3 days for a voiding trial. He failed the voiding trial, and personnel at the local hospital were unable to replace the catheter. He was referred to our institution for further management. Physical examination reveals normal Sexual Maturity Rating stage 1 genitalia and a palpable bladder. He does not have any sacral dimples. Efforts to pass a 5-French feeding tube through the urethra also fail. Additional history and an imaging procedure lead to the diagnosis. The neurology consultant examines a 2-year-old boy in the outpatient clinic for “passing-out seizures.” His mother indicates that, in response to loud sounds, her otherwise healthy child experiences episodes of generalized, nonrhythmic, tonic muscle contractions characterized by “stiffness and back-arching,” collapse, and apnea. The episodes last 30 to 45 seconds, and in a typical day, the boy experiences three to four events. No other family members experience similar bouts. Findings on ECG, echocardiography, and 23-hour cardiac monitoring are unremarkable. Physical examination reveals an alert toddler who interacts appropriately with his mother and has no obvious signs of sensory or motor deficit. To evaluate the events, the child is admitted to the epilepsy monitoring unit. Examination of the electroencephalogram (EEG) reveals normal background rhythm. During the …
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