Wolff-Parkinson-White syndrome, childhood-onset

MedGen UID:: 865246
•Concept ID:: C4016809
•: Finding

Synonym:	WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET

OMIM®:	602743

Recent clinical studies

Prognosis

Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.

Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, Roberts R
Circulation 2001 Dec 18;104(25):3030-3. doi: 10.1161/hc5001.102111. PMID: 11748095

See all (1)

Clinical prediction guides

Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.

Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, Roberts R
Circulation 2001 Dec 18;104(25):3030-3. doi: 10.1161/hc5001.102111. PMID: 11748095

See all (1)

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Wolff-Parkinson-White syndrome, childhood-onset

Recent clinical studies

Prognosis

Clinical prediction guides

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