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A Case of Hydrometrocolpos and Polydactyly

机译:一例大肠积水和多发性

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摘要

Neonatal hydrometrocolpos (HMC) is a rare Mullerian duct anomaly with an incidence of 0.006%. It occurs due to blockage of the vagina with accumulation of mucus secretions proximal to the obstacle. These secretions are secondary to intrauterine and postnatal stimulation of uterine and cervical glands by maternal estrogens. A triad of congenital HMC, polydactyly, and cardiac anomalies are the cardinal features of McKusick–Kaufman syndrome, which is also known as hydrometrocolpos-polydactyly syndrome. Bardet–Biedl syndrome is a well-known combination of hypogonadism, obesity, postaxial polydactyly, renal dysplasia, retinal degeneration, and mental impairment. In this case report, we describe a neonate with HMC, polydactyly, and hydronephrosis.
机译:新生儿积水(HMC)是一种罕见的苗勒氏管畸形,发生率为0.006%。它的发生是由于阴道阻塞,并在障碍物附近堆积了粘液分泌物。这些分泌物是继发于宫内和产后雌激素刺激子宫和子宫颈的产后。先天性HMC,多指畸形和心脏畸形的三联征是McKusick-Kaufman综合征的主要特征,该综合征也被称为输尿管结肠多指综合征。 Bardet–Biedl综合征是性腺机能减退,肥胖,后轴多指,肾发育不良,视网膜变性和精神障碍的众所周知的组合。在此病例报告中,我们描述了具有HMC,多指和肾积水的新生儿。

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