Hydrolethalus Syndrome: A Case of a Rare Congenital Disorder.

IF 3.8 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Diagnostics Pub Date : 2025-01-17 DOI:10.3390/diagnostics15020202
Valerica Belengeanu, Diana Marian, Horia Ademir Stana, Carolina Cojocariu, Cristina Popescu, Ioana Elena Lile
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Abstract

This is a fatal case of multiple complicated congenital anomalies displaying several symptoms consistent with hydrolethalus syndrome. The newborn's phenotype is characterized by a combination of serious anatomical abnormalities such as open-book cerebral hemispheres, defective lobulation of the lungs (one lobe on the left, two on the right), a smaller right kidney, a smooth cerebral surface, and a specific keyhole-shaped defect in the skull base, primarily associated with hydrocephalus.

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足部积液综合征:一例罕见的先天性疾病。
这是一个致命的病例,多重复杂的先天性异常,表现出与足部积水综合征一致的几种症状。新生儿表型的特点是严重的解剖异常,如大脑半球呈开卷状,肺分叶有缺陷(左一肺,右两肺),右肾较小,大脑表面光滑,颅底有特定的锁眼状缺陷,主要与脑积水有关。
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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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