1. A case of pregnancy complicated with dilated cardiomyopathy 1X
- Author
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Tomoyuki Fujii, Atsushi Komatsu, Takayuki Iriyama, Takeshi Nagamatsu, Yutaka Osuga, and Shinya Oki
- Subjects
Cardiac function curve ,Pregnancy ,medicine.medical_specialty ,Pediatrics ,Ejection fraction ,business.industry ,medicine.medical_treatment ,Dilated cardiomyopathy ,Case Reports ,medicine.disease ,Bed rest ,Compound heterozygosity ,Microbiology ,Fukutin ,Infectious Diseases ,Internal medicine ,medicine ,Cardiology ,cardiovascular system ,Gestation ,Parasitology ,business - Abstract
Dilated cardiomyopathy 1X (CMD1X) is characterized by dilated cardiomyopathy (DCM) with mildest limb-girdle muscle symptoms and normal intelligence. Compound heterozygous mutation in fukutin gene is known as its genetic cause. Here, we report a pregnancy case complicated with CMD1X. A 25-year-old primiparous woman, who had been diagnosed as CMD1X at the age of 19, was referred to our hospital at 6 weeks of gestation. In early pregnancy, the evaluation of her cardiac function showed ejection fraction 47% and NYHA class II. Worsening of cardiac function was observed from 30 weeks, manifesting reduced cardiac load with left ventricular dilatation and in-hospital bed rest was necessary. Elective cesarean section was performed at 35 weeks to prevent deterioration of cardiac function. The parameters of her cardiac function returned to the pre-pregnancy status in a month after delivery, whereas she realized persistent worsening of muscular weakness at postpartum.
- Published
- 2015