[Potter sequence in a newborn with polycystic kidney disease].

Q4 Medicine Arkhiv patologii Pub Date : 2024-01-01 DOI:10.17116/patol20248601149
N S Averkin, T V Pryazhentseva, A P Stolyarov, E A Kharitonov, I V Rybakova
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引用次数: 0

Abstract

A rare clinical case of a newborn boy with a diagnosed Potter sequence is presented. The diagnosis was made based on polycystic dysplasia of the kidneys, cysts in the liver, hypoplasia of the lungs and characteristic external signs due to critical oligohydramnios. The child's parents were closely related, which suggested an autosomal recessive form of the disease. The newborn lived for 15 hours, after which the death, developed as a result of respiratory failure, was ascertained.

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[多囊肾新生儿的波特序列]。
本报告介绍了一个罕见的临床病例,该病例是一名被诊断为波特序列的新生男婴。诊断依据是肾脏多囊发育不良、肝脏囊肿、肺发育不全以及临界少尿症导致的特征性外部体征。孩子的父母关系密切,这表明该病是一种常染色体隐性遗传病。新生儿存活了 15 个小时,之后因呼吸衰竭死亡。
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来源期刊
Arkhiv patologii
Arkhiv patologii Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
55
期刊介绍: The journal deals with original investigations on pressing problems of general pathology and pathologic anatomy, newest research methods, major issues of the theory and practice as well as problems of experimental, comparative and geographic pathology. To inform readers latest achievements of Russian and foreign medicine the journal regularly publishes editorial and survey articles, reviews of the most interesting Russian and foreign books on pathologic anatomy, new data on modern methods of investigation (histochemistry, electron microscopy, autoradiography, etc.), about problems of teaching, articles on the history of pathological anatomy development both in Russia and abroad.
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