Biomaterial Database

LEOPARD syndrome with Wolff-Parkinson-White syndrome on electrocardiography. 2013

Sangita Ghosh, and Soumik Chaudhuri, and Vijay Kumar Jain

Department of Skin and Veneral Diseases, Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India.

UI	MeSH Term	Description	Entries
D004562	Electrocardiography	Recording of the moment-to-moment electromotive forces of the HEART as projected onto various sites on the body's surface, delineated as a scalar function of time. The recording is monitored by a tracing on slow moving chart paper or by observing it on a cardioscope, which is a CATHODE RAY TUBE DISPLAY.	12-Lead ECG,12-Lead EKG,12-Lead Electrocardiography,Cardiography,ECG,EKG,Electrocardiogram,Electrocardiograph,12 Lead ECG,12 Lead EKG,12 Lead Electrocardiography,12-Lead ECGs,12-Lead EKGs,12-Lead Electrocardiographies,Cardiographies,ECG, 12-Lead,EKG, 12-Lead,Electrocardiograms,Electrocardiographies, 12-Lead,Electrocardiographs,Electrocardiography, 12-Lead
D005260	Female		Females
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293	Adolescent	A person 13 to 18 years of age.	Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D014927	Wolff-Parkinson-White Syndrome	A form of ventricular pre-excitation characterized by a short PR interval and a long QRS interval with a delta wave. In this syndrome, atrial impulses are abnormally conducted to the HEART VENTRICLES via an ACCESSORY CONDUCTING PATHWAY that is located between the wall of the right or left atria and the ventricles, also known as a BUNDLE OF KENT. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated protein kinase.	WPW Syndrome,Anomalous Ventricular Excitation Syndrome,Auriculoventricular Accessory Pathway Syndrome,False Bundle-Branch Block Syndrome,Ventricular Pre-Excitation with Arrhythmia,Wolf-Parkinson-White Syndrome,Syndrome, WPW,Syndrome, Wolf-Parkinson-White,Syndrome, Wolff-Parkinson-White,Wolf Parkinson White Syndrome,Wolff Parkinson White Syndrome
D044542	LEOPARD Syndrome	An autosomal dominant disorder with an acronym of its seven features (LENTIGO; ELECTROCARDIOGRAM abnormalities; ocular HYPERTELORISM; PULMONARY STENOSIS; abnormal genitalia; retardation of growth; and DEAFNESS or SENSORINEURAL HEARING LOSS). This syndrome is caused by mutations of PTPN11 gene encoding the non-receptor PROTEIN TYROSINE PHOSPHATASE, type 11, and is an allelic to NOONAN SYNDROME. Features of LEOPARD syndrome overlap with those of NEUROFIBROMATOSIS 1 which is caused by mutations in the NEUROFIBROMATOSIS 1 GENES.	Cardio-Cutaneous Syndrome,Cardiomyopathic Lentiginosis,LEOPARD Syndrome, 1,Lentiginosis Cardiomyopathic,Leopard Syndrome 1,Multiple Lentigines Syndrome,Noonan Syndrome with Multiple Lentigines,Progressive Cardiomyopathic Lentiginosis,Cardio Cutaneous Syndrome,Cardio-Cutaneous Syndromes,Cardiomyopathic Lentiginoses,Cardiomyopathic Lentiginoses, Progressive,Cardiomyopathic Lentiginosis, Progressive,Cardiomyopathic, Lentiginosis,Cardiomyopathics, Lentiginosis,LEOPARD Syndromes,Lentigines Syndrome, Multiple,Lentigines Syndromes, Multiple,Lentiginoses, Cardiomyopathic,Lentiginoses, Progressive Cardiomyopathic,Lentiginosis Cardiomyopathics,Lentiginosis, Cardiomyopathic,Lentiginosis, Progressive Cardiomyopathic,Multiple Lentigines Syndromes,Progressive Cardiomyopathic Lentiginoses,Syndrome, Cardio-Cutaneous,Syndrome, LEOPARD,Syndrome, Multiple Lentigines,Syndromes, Cardio-Cutaneous,Syndromes, LEOPARD,Syndromes, Multiple Lentigines