Tetralogy of Fallot with Holt-Oram syndrome

Indian Heart Journal

Volumn 64, Issue 1, 2012, Pages 95-98

  Kumar, Vikas ^a   Agrawal, Vikas ^a   Jain, Dharmendra ^a   Shankar, Om ^a  

^a BANARAS HINDU UNIVERSITY   (India)

Author keywords

Arrhythmias; Atrial septal defect; Holt Oram syndrome; Tetralogy of Fallot

Indexed keywords

HEMOGLOBIN;

ARTICLE; CARDIOVASCULAR SYSTEM EXAMINATION; CASE REPORT; CHILD; CLUBBING FINGERS; COLOR ULTRASOUND FLOWMETRY; CYANOSIS; DISEASE ASSOCIATION; ELECTROCARDIOGRAM; FALLOT TETRALOGY; FATIGUE; FEMALE; GROWTH RETARDATION; HAND MALFORMATION; HEART RIGHT LEFT SHUNT; HEART RIGHT VENTRICLE HYPERTROPHY; HEART VENTRICLE SEPTUM DEFECT; HOLT ORAM SYNDROME; HUMAN; HYPOPLASIA; LEVOCARDIA; MUSCULOSKELETAL SYSTEM EXAMINATION; PERIMEMBRANOUS HEART VENTRICLE SEPTUM DEFECT; PRESCHOOL CHILD; PULMONARY VALVE STENOSIS; RADIAL DEVIATION; SYSTOLIC HEART MURMUR; THORAX RADIOGRAPHY; THREE DIMENSIONAL ECHOCARDIOGRAPHY; THUMB HYPOPLASIA; VALGUS DEFORMITY;

EID: 84861592153     PISSN: 00194832     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0019-4832(12)60021-2     Document Type: Article

References (5)

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3. Li QY, Newbury-Ecob RA, Terrett JA, et al. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Nat Genet 1997;15:21-9.
4. Weber M, Wenz W, van Riel A, et al. The Holt-Oram syndrome. Review of the literature and current orthopaedic treatment concepts. Z Orthop Ihre Grenzgeb 1997;135:368-75.
5. Sletten LJ, Pierpont ME. Variation in severity of cardiac disease in Holt-Oram syndrome. Am J Med Genet 1996;65:128-32.