A novel MYH7 gene mutation in a fetus with left ventricular noncompaction

Canadian Journal of Cardiology

Volumn 31, Issue 1, 2015, Pages 103.e1-103.e3

  Nomura, Yasuhisa ^a   Momoi, Nobuo ^a   Hirono, Keiichi ^b   Hata, Yukiko ^b   Takasaki, Asami ^b   Nishida, Naoki ^b   Ichida, Fukiko ^b  

^a FUKUSHIMA MEDICAL UNIVERSITY   (Japan)

^b UNIVERSITY OF TOYAMA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MYOSIN HEAVY CHAIN BETA; CARDIAC MYOSIN; MYH7 PROTEIN, HUMAN; MYOSIN HEAVY CHAIN;

ADULT; ARTICLE; ASCITES; AUTOPSY; CARDIOMEGALY; CASE REPORT; CONTROLLED STUDY; ECHOCARDIOGRAPHY; ENDOCARDIAL FIBROELASTOSIS; FEMALE; FETUS; FETUS ECHOGRAPHY; FETUS HYDROPS; GENETIC VARIABILITY; HEART DILATATION; HEART VALVE REGURGITATION; HUMAN; HUMAN TISSUE; HYPOKINESIA; MALE; MISSENSE MUTATION; NEWBORN; PATHOGENESIS; PLEURA EFFUSION; PRIMIGRAVIDA; SECOND TRIMESTER PREGNANCY; SINGLE NUCLEOTIDE POLYMORPHISM; STILLBIRTH; VENTRICULAR NONCOMPACTION; BIOPSY; EMBRYOLOGY; GENETICS; HEART MUSCLE; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; METABOLISM; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PREGNANCY; PRENATAL DIAGNOSIS;

ADULT; BIOPSY; CARDIAC MYOSINS; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; MUTATION; MYOCARDIUM; MYOSIN HEAVY CHAINS; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84920414923     PISSN: 0828282X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cjca.2014.11.012     Document Type: Article

References (5)

1. Ichida F. Left ventricular noncompaction. Circ J 2009, 73:19-26.
2. Menon S.C., O'Leary P.W., Wright G.B., et al. Fetal and neonatal presentation of noncompacted ventricular myocardium; expanding the clinical spectrum. JAm Soc Echocardiogr 2007, 20:1344-1350.
3. Hoedemaekers Y.M., Cohen-Overbeek T.E., Frohn-Mulder I.M., et al. Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy. Ultrasound Obstet Gynecol 2013, 41:336-339.
4. Ozkutlu S., Bostan O., Karagöz T., et al. Prenatal diagnosis of isolated non-compaction of the ventricular myocardium: study of six cases. Pediatr Int 2007, 49:172-176.
5. Hoedemaekers Y.M., Caliskan K., Michels M., et al. The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy. Circ Cardiovasc Genet 2010, 3:232-239.