Rare Extracardiac Anomalies Presented with Right Heterotaxy Syndrome in a Newborn Baby: A Case Report

被引:0
作者
Huseynova, Roya [1 ]
Bin Mahmoud, Latifa A. [1 ]
AlJohani, Eman [1 ]
Huseynov, Oqtay [2 ]
Abdelrahim, Adli [1 ]
AlOmran, Khalid A. [3 ]
机构
[1] King Saud Med City, Dept Neonatol, Riyadh, Saudi Arabia
[2] Azerbaijan Med Univ, Baku, Azerbaijan
[3] King Saud Med City, Dept Cardiol, Riyadh, Saudi Arabia
关键词
Heterotaxy Syndrome; Infant; Newborn; Isomerism; ASPLENIA SYNDROME; PREVENTION; DEFECTS; ABSENT;
D O I
10.12659/AJCR.923341
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Unusual clinical course Background: Heterotaxy is a syndrome of abnormal arrangement of the internal thoracic-abdominal structures across the left-right axis of the body. It is a primary disorder with 2 main settings - bilateral left sidedness (polysplenia syndrome) or right sidedness (asplenia syndrome) - although some overlapping or uncertainties may occur. Patients with right heterotaxy typically present with asplenia, complex heart disease, and other thoracoabdominal organ situs abnormalities. Case Report: We present a unique case of congenital asplenia syndrome with complex heart disease, annular pancreas, and other extra-heterotaxic anomalies (e.g., musculoskeletal) in the form of a radius aplasia and partial syndactyly of the thumb and index finger of the left hand. These associated anomalies have not been reported before. Conclusions: This case shows the need for paying increased attention to the implications of other extracardiac anomalies that can be associated with heterotaxy syndrome.
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页码:1 / 5
页数:5
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