合并复杂先天性心脏病、面瘫和无脾的内脏异位综合征：一种罕见的新生儿表现。
Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding.
作者信息
Kharel Sanjeev, Koirala Dinesh Prasad, Shrestha Suraj, Sedai Hari, Shrestha Bibek Man, Homagain Sushan, Kandel Suraj
机构信息
Institute of Medicine Maharajgunj Medical Campus Kathmandu Nepal.
Department of Gastrointestinal and General Surgery Pediatric Surgery Unit Tribhuvan University Teaching Hospital Kathmandu Nepal.
出版信息
Clin Case Rep. 2021 Aug 7;9(8):e04573. doi: 10.1002/ccr3.4573. eCollection 2021 Aug.
Heterotaxy syndrome is associated with asplenia/polysplenia and complex congenital heart disease. Facial palsy in heterotaxy is very rare. The management is still challenging with a poor prognosis. Proper counseling to the family about the disease course, treatment modalities, and outcomes is essential.
内脏反位综合征与无脾/多脾及复杂先天性心脏病相关。内脏反位患者出现面神经麻痹非常罕见。其治疗仍然具有挑战性，预后较差。向家属就疾病进程、治疗方式及预后进行恰当的咨询至关重要。
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