Novel MYH7 Variant in the Neonate of a Mother with Gestational Diabetes Mellitus Showing Left Ventricular Hypertrophy and Noncompaction

被引:1
|
作者
Ozawa, Sayaka W. [1 ]
Inomata, Satomi [1 ]
Hata, Yukiko [2 ]
Takarada, Shinya [1 ]
Okabe, Mako [1 ]
Nakaoka, Hideyuki [1 ]
Ibuki, Keijiro [1 ]
Nishida, Naoki [2 ]
Ichida, Fukiko [3 ]
Hirono, Keiichi [1 ]
机构
[1] Univ Toyama, Fac Med, Dept Pediat, Toyama 9300194, Japan
[2] Univ Toyama, Fac Med, Legal Med, Toyama 9300194, Japan
[3] Int Univ Hlth & Welf, Dept Pediat, Tokyo 1070052, Japan
关键词
gestational diabetes mellitus; left ventricular noncompaction; MYH7; gene; NON-COMPACTION;
D O I
10.3390/genes15030381
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Left ventricular hypertrophy (LVH) is a well-recognized cardiac dysfunction in infants of mothers with gestational diabetes mellitus (GDM). Left ventricular noncompaction (LVNC) is a cardiomyopathy that is morphologically characterized by numerous prominent trabeculations and deep intertrabecular recesses on cardiovascular imaging. However, there have been no case reports on neonates of mothers with GDM showing LVH and LVNC. Case presentation: A patient, with LVH of a mother with GDM, was delivered at 36 weeks of gestation. Prominent trabeculations in the LV, suggesting LVNC, instead of LVH, were apparent 1 week after birth. A heterozygous deletion variant in the MYH7 gene (NM_000257.4: c.1090T>C, p.Phe364Leu) was discovered through genetic testing using a cardiomyopathy-associated gene panel in the patient and his father and the older brother who had LVNC. The patient is now 5 years old and does not have major cardiac events, although LVNC persisted. This is the first case of LVH secondary to a mother with GDM and LVNC with a novel variant in the MYH7 gene. Conclusion: Genetic testing should be conducted to obtain an accurate outcome and medical care in a patient with LVH and subsequently prominent hypertrabeculation in the LV.
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页数:9
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