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Iranian Journal of Neonatology، جلد ۱۱، شماره ۴، صفحات ۱۱۴-۱۱۸
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Isolated Right Ventricular Non-compaction in a Neonate Born to a Mother with Gestational Diabetes: A Case Report |
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| چکیده انگلیسی مقاله |
Background: Ventricular non-compaction, which is a rare congenital cardiomyopathy, results from an arrest in normal endomyocardial embryogenesis. It is characterized by a pattern of prominent trabecular meshwork and deep inter-trabecular recesses. The clinical manifestations include systolic and diastolic dysfunctions, heart failure, ventricular arrhythmias, and cardioembolic events.Case report: Here we present the case of a neonate (38 weeks, weighing 2580 gr) born to a mother with gestational diabetes (GDM) with isolated right ventricular non-compaction (IRVNC) and systolic and diastolic right heart dysfunction due to meconium aspiration syndrome and tension pneumothorax. A 4-month follow-up demonstrated a complete improvement in the newborn.Conclusion: It is of paramount importance to consider RVNC cardiomyopathy a differential diagnosis of cyanosis and respiratory distress due to meconium aspiration syndrome in neonate s born to mothers with GDM. Apart from RV cardiac dysfunction, RVNC could cause such complications as pulmonary hypertension and tension pneumothorax. It can be also spontaneously improved in GMD. |
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| کلیدواژه‌های انگلیسی مقاله |
Cardiomyopathy, Gestational diabetes, Newborn, Right Ventricular Non-Compaction, Tension Pneumothorax |
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| نویسندگان مقاله |
| Yazdan Ghandi
Amir Kabir Hospital, Arak University of Medical Sciences, Arak, Iran
| Sarvenaz Mehrabi
Department of Emergency, School of Medicine, Arak University of Medical Sciences, Arak, Iran
| Saeed Alinejad
Department of Pediatrics, School of Medicine, Amir Kabir Hospital, Arak University of Medical Sciences, Arak, Iran
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| نشانی اینترنتی |
https://ijn.mums.ac.ir/article_16322.html |
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| زبان مقاله منتشر شده |
en |
| موضوعات مقاله منتشر شده |
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| نوع مقاله منتشر شده |
گزارش موارد نادر |
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