TY - JOUR
T1 - Secondary enuresis and urological manifestations in children with ataxia telangiectasia
AU - Nissenkorn, Andreea
AU - Erlich, Tomer
AU - Zilberman, Dorit E.
AU - Sarouk, Ifat
AU - Krauthammer, Alexander
AU - Kitrey, Noam D.
AU - Heimer, Gali
AU - BenZeev, Bruria
AU - Mor, Yoram
N1 - Publisher Copyright:
© 2018 European Paediatric Neurology Society
PY - 2018/11
Y1 - 2018/11
N2 - Background: Ataxia telangiectasia (AT) is a neurodegenerative cerebellar disorder, caused by mutations in the ATM gene, involved in DNA repair. Radiosensitivity, progressive ataxia, immune deficiency and malignancies, are well known symptoms, but urological manifestations are scarcely described. Objective: To characterize urologic manifestations in a large cohort of AT patients. Methods: Retrospective cross-sectional chart study comprising 52 AT patients followed at a National AT Center. Results: 25% of the cohort (13 patients/8 males) had urologic symptoms, which presented at 11 ± 4.3 years. The most common symptom was secondary enuresis affecting 15% of the patients (8 children/4 males). Incontinence appeared at 8 ± 6.2 years of age, and resolved spontaneously within 15 ± 8.3 months in 6 patients. It preceded loss of ambulatory capacity by 1–2 years in 7 patients. Lumbosacral MRI were normal (4 children) and urine cultures (all) were negative. Urodynamic evaluation that was performed in only one patient revealed overactive bladder. Additional manifestations were macroscopic hematuria due to bladder telangiectasia in a 12-year-old, and renal cell carcinoma in a 22-year-old. Other manifestations unrelated to AT were neprolithiasis, vesico-ureteral reflux and scrotal pain, each in 1 patient. Discussion: Transient secondary enuresis is a frequent finding in AT patients, heralding loss of ambulatory capacity, tough it's pathophysiological mechanism is largely no understood.
AB - Background: Ataxia telangiectasia (AT) is a neurodegenerative cerebellar disorder, caused by mutations in the ATM gene, involved in DNA repair. Radiosensitivity, progressive ataxia, immune deficiency and malignancies, are well known symptoms, but urological manifestations are scarcely described. Objective: To characterize urologic manifestations in a large cohort of AT patients. Methods: Retrospective cross-sectional chart study comprising 52 AT patients followed at a National AT Center. Results: 25% of the cohort (13 patients/8 males) had urologic symptoms, which presented at 11 ± 4.3 years. The most common symptom was secondary enuresis affecting 15% of the patients (8 children/4 males). Incontinence appeared at 8 ± 6.2 years of age, and resolved spontaneously within 15 ± 8.3 months in 6 patients. It preceded loss of ambulatory capacity by 1–2 years in 7 patients. Lumbosacral MRI were normal (4 children) and urine cultures (all) were negative. Urodynamic evaluation that was performed in only one patient revealed overactive bladder. Additional manifestations were macroscopic hematuria due to bladder telangiectasia in a 12-year-old, and renal cell carcinoma in a 22-year-old. Other manifestations unrelated to AT were neprolithiasis, vesico-ureteral reflux and scrotal pain, each in 1 patient. Discussion: Transient secondary enuresis is a frequent finding in AT patients, heralding loss of ambulatory capacity, tough it's pathophysiological mechanism is largely no understood.
KW - ATM
KW - Ataxia telangiectasia
KW - Incontinence
KW - Neurogenic bladder
KW - Urinary tract
UR - http://www.scopus.com/inward/record.url?scp=85051101574&partnerID=8YFLogxK
U2 - 10.1016/j.ejpn.2018.07.006
DO - 10.1016/j.ejpn.2018.07.006
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C2 - 30100180
AN - SCOPUS:85051101574
SN - 1090-3798
VL - 22
SP - 1118
EP - 1123
JO - European Journal of Paediatric Neurology
JF - European Journal of Paediatric Neurology
IS - 6
ER -