Zinner syndrome: a rare diagnosis in infancy.

Autor:	Rose JMO; Urology, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, Coventry, UK., Banthia R; Urology, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, Coventry, UK.; Urology and Renal Transplantation, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India., Tamboli Z; Urology and Renal Transplantation, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India., Lal H; Radiodiagnosis, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India hiralal2007@yahoo.co.in.
Jazyk:	angličtina
Zdroj:	BMJ case reports [BMJ Case Rep] 2022 May 19; Vol. 15 (5). Date of Electronic Publication: 2022 May 19.
DOI:	10.1136/bcr-2021-248558
Abstrakt:	We present a case of Zinner syndrome (ZS), where we were fortunate to diagnose a child with this rare syndrome immediately after birth. Gross hydronephrosis was observed during the prenatal period on ultrasound, and further imaging after birth confirmed the presence of a multicystic dysplastic kidney and seminal vesicle cyst. The majority of cases of ZS is asymptomatic; however, symptoms relating to urination, ejaculation or infertility may present later on in life and so regular follow-up is required to ensure interventions can be carried out if such symptoms do occur. Competing Interests: Competing interests: None declared. (© BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.)
Databáze:	MEDLINE
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