与卵圆孔未闭有关的努南综合征

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Nigerian Postgraduate Medical Journal Pub Date : 2025-01-01 Epub Date: 2025-03-17 DOI:10.4103/npmj.npmj_294_24
Oyewole Adebiyi Kushimo, Ogochukwu Jidechukwu Sokunbi, Festus Ibe, Ayodeji S Adekolade
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引用次数: 0

摘要

努南综合征是一种以面部、肌肉骨骼和心血管系统异常为特征的遗传性疾病。肺狭窄是最常见的异常。我们描述了一个48岁的男性与努南综合征的临床特征,和严重的肺狭窄与紫绀。从儿童时期起就注意到长期的努力不容忍史。发绀的原因尚不清楚,因为最初的回声没有显示明显的多普勒成像分流。一项激动生理盐水对比研究证实了卵圆孔未闭(PFO)伴右至左分流。在患有努南综合征和不明原因发绀的患者中,应怀疑和筛查PFO。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Noonan Syndrome Associated with a Patent Foramen Ovale.

Noonan syndrome is a genetic disorder characterised by abnormalities of the facial, musculoskeletal and cardiovascular systems. Pulmonary stenosis is the most common abnormality seen. We describe a 48-year-old male with clinical features of Noonan syndrome, and severe pulmonary stenosis with cyanosis. A long-standing history of effort intolerance was noted since childhood. The cause of cyanosis was unclear since an initial echo did not reveal an obvious shunt by Doppler imaging. An agitated saline contrast study performed confirmed a patent foramen ovale (PFO) with right to left shunting. PFO should be suspected and screened for in patients with Noonan syndrome and unexplained cyanosis.

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来源期刊
Nigerian Postgraduate Medical Journal
Nigerian Postgraduate Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
1.90
自引率
0.00%
发文量
52
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