LEOPARD syndrome in an infant with severe hypertrophic cardiomyopathy and PTPN11 mutation

Annals of Pediatric Cardiology

Volumn 4, Issue 1, 2011, Pages 74-76

  Ganigara, Madhusudan ^a   Prabhu, Atul ^a   Kumar, Raghvannair Suresh ^a  

^a Madras Medical Mission ^*  (India)

Author keywords

Hypertrophic cardiomyopathy; lentiginosis; LEOPARD syndrome; PTPN11 mutation

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; GLUTAMIC ACID; PROTEIN TYROSINE PHOSPHATASE; PROTEIN TYROSINE PHOSPHATASE SHP 2;

ARTICLE; CASE REPORT; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; EXON; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENOTYPE PHENOTYPE CORRELATION; HEART LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; INFANT; LEOPARD SYNDROME; LIQUID CHROMATOGRAPHY; MALE; POLYMERASE CHAIN REACTION; SURGERY; THORAX RADIOGRAPHY;

EID: 79955409300     PISSN: 09742069     EISSN: 09745149     Source Type: Journal    
DOI: 10.4103/0974-2069.79631     Document Type: Article

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