Proximal trisomy of 1q mosaicism in a girl with hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome and multiple congenital anomalies

2001 ◽  
Vol 100 (4) ◽  
pp. 264-268 ◽  
Author(s):  
Amy B. Hirshfeld ◽  
W. Reid Thompson ◽  
Ankita Patel ◽  
Lucy Barrett Boone ◽  
Anne M. Murphy
Keyword(s):  
Hypertrophic Cardiomyopathy ◽  
Congenital Anomalies ◽  
Multiple Congenital Anomalies ◽  
White Syndrome ◽  
Wolff Parkinson White Syndrome

Mutation of theMYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome

2007 ◽  
Vol 48 (2) ◽  
pp. 185-188 ◽  
Author(s):  
Waldemar Bobkowski ◽  
Małgorzata Sobieszczańska ◽  
Anna Turska-Kmieć ◽  
Agnieszka Nowak ◽  
Józef Jagielski ◽  
...  
Keyword(s):  
Hypertrophic Cardiomyopathy ◽  
White Syndrome ◽  
Wolff Parkinson White Syndrome

scholarly journals Hypertrophic Cardiomyopathy and Wolff-Parkinson-White Syndrome in a Young African Soldier with Recurrent Syncope

2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Mohammed Abdullahi Talle ◽  
Faruk Buba ◽  
Aimé Bonny ◽  
Musa Mohammed Baba
Keyword(s):  
Atrial Fibrillation ◽  
Ventricular Tachycardia ◽  
Hypertrophic Cardiomyopathy ◽  
General Population ◽  
Supraventricular Tachycardia ◽  
White Syndrome ◽  
Wpw Syndrome ◽  
The Individual ◽  
Common Manifestation ◽  
Wolff Parkinson White Syndrome

Syncope is a common manifestation of both hypertrophic cardiomyopathy (HCM) and Wolff-Parkinson-White (WPW) syndrome. The most common arrhythmia in HCM is ventricular tachycardia (VT) and atrial fibrillation (AF). While preexcitation provides the substrate for reentry and supraventricular tachycardia (SVT), AF is more common in patients with preexcitation than the general population. Concurrence of HCM and WPW has been reported in many cases, but whether the prognosis or severity of arrhythmia is different compared to the individual disorders remains unsettled. We report a case of HCM and Wolff-Parkinson-White (WPW) syndrome in a 28-year-old male Nigerian soldier presenting with recurrent syncope and lichen planus.

scholarly journals Hypertrophic Cardiomyopathy due to Mitochondrial Disease: Prenatal Diagnosis, Management, and Outcome

2013 ◽  
Vol 2013 ◽  
pp. 1-4
Author(s):  
Lutgardo García-Díaz ◽  
Félix Coserria ◽  
Guillermo Antiñolo
Keyword(s):  
Prenatal Diagnosis ◽  
Hypertrophic Cardiomyopathy ◽  
Congenital Heart ◽  
Left Ventricular ◽  
First Year ◽  
Mitochondrial Oxidative Phosphorylation ◽  
White Syndrome ◽  
Skeletal Muscle Biopsy ◽  
First Year Of Life ◽  
Wolff Parkinson White Syndrome

A case of prenatally diagnosed fetal hypertrophic cardiomyopathy is reported. The mother was referred to our department at 37 weeks' gestation because of suspected congenital heart disease. Prenatal echocardiography showed biventricular hypertrophy and pericardial effusion, without additional abnormalities. Postnatal echocardiography confirmed prenatal diagnosis. Neonatal EKG showed biventricular hypertrophy and Wolff-Parkinson-White syndrome. Skeletal muscle biopsy was consistent with mitochondrial oxidative phosphorylation defect involving a combined defect of respiratory complexes I and IV. Echocardiographic followup during the first year of life showed progressive regression of hypertrophy and evolution to left ventricular myocardial noncompaction.

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