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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review

Fig. 1

(A) Pedigree chart of the family of the patient with dilated cardiomyopathy type-2D. The proband is indicated by a black arrow. (B)-(C) Chest and abdominal X-ray showing severe cardiomegaly and intestinal obstruction at presentation. (D) M-mode echocardiography displaying depressed LV systolic function (LVSF 12%). (E)-(F) Electrocardiogram showing T segmentchanges and first degree atrioventricular block. (G)-(H) 24-hour EKG monitoring showing occasional premature atrial contractions and paroxysmal ST segment changes

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