Wrist and Hand Conditions

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Congenital LQTS is predominantly a hereditary disorder, usually transmitted in an AD manner. In a smaller number of affected subjects, transmission is AR and associated with sensorineural deafness. This disorder is associated with torsade de pointes, usually precipitated by emotional circumstances and/or physical activity, and presents clinically with syncope and sudden death.
LQTS is a relatively rare cause of sudden death in young individuals, including athletes, and usually occurs in subjects with a history of recurrent syncope. Sudden death has been found in family members and carriers of LQTS who do not show long QT intervals on their resting 12-lead ECG. Exclusion from all competitive sports.
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Sudden Cardiac Death in Athletes Fa
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Other definitions limit the time fr
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History The first recorded sudden d
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professional basketball All-Star Re
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Landmark studies Maron et al: 134 S
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France Institute of Forensic Medici
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Etiology (Brukner) Common: Hypertro
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Etiology USA Hypertrophic cardiomyo
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Italy To establish the impact of sp
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France 31 SCDs: 29 male subjects, r
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Among non sports-related SCDs in th
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Hypertrophic cardiomyopathy is gene
Page 30 and 31:
Unfortunately, often the first clin
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Physical Findings Rapid, jerky upst
Page 34 and 35: Note: Elite athletes with left vent
Page 36 and 37: Electrocardiographic Findings drama
Page 38 and 39: Apical hypertrophic cardiomyopathy.
Page 40 and 41: Recommendations for diagnostic eval
Page 43 and 44: Recommendations for participation i
Page 45 and 46: Nonpharmacologic therapies are rese
Page 48 and 49: Coronary Artery Anomalies The secon
Page 50: Anatomy - Coronary Arteries
Page 53 and 54: Both MRI and CT coronary angiograph
Page 55 and 56: Myocarditis Is frequently the resul
Page 57 and 58: Endomyocardial biopsy and histologi
Page 59 and 60: Arrhythmogenic right ventricular dy
Page 61 and 62: The first clinical sign of ARVD is
Page 63 and 64: ECG changes in the majority of case
Page 66: Criteria for the differential diagn
Page 69 and 70: Wolff-Parkinson-White syndrome An a
Page 71 and 72: The resting ECG may demonstrate an
Page 73 and 74: WPW
Page 75 and 76: Brugada syndrome A syndrome of SCD
Page 78 and 79: Brugada syndrome. Note the incomple
Page 80 and 81: Determination of the QT interval. O
Page 82 and 83: Long QT Syndrome
Page 84: V-tach that changes orientation (ch
Page 89 and 90: Aortic rupture Aortic rupture makes
Page 91 and 92: Common manifestations involve the s
Page 93 and 94: Diagnosis Positive family history:
Page 95 and 96: Commotio cordis or cardiac concussi
Page 97 and 98: Exposure to agents such as erythrom
Page 100 and 101: Preventive Strategies American appr
Page 102 and 103: Family history 6. Premature death (
Page 104 and 105: Prehospital Care Time period betwee
Page 106: Cardiopulmonary resuscitation shoul
Page 109 and 110: 4. Tanaka Y, Yoshinaga M, Anan R, T
Page 111 and 112: 10. Fornes P, Lecomte D. Pathology
Page 113 and 114: 16. Wren C. Sudden death in childre
Page 115 and 116: Questions??
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