Symptomatic liver involvement in neonatal hereditary hemorrhagic telangiectasia

Pediatrics

Volumn 127, Issue 6, 2011, Pages

  Al Saleh, Suhail ^a,b,c,d   John, Philip R ^a,b   Letarte, Michelle ^a,b   Faughnan, Marie E ^a,e,f   Belik, Jaques ^b,c   Ratjen, Felix ^a,b,c  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^d KING SAUD BIN ABDULAZIZ UNIVERSITY FOR HEALTH SCIENCES   (Saudi Arabia)

^e ST MICHAEL'S HOSPITAL   (Canada)

^f ST MICHAEL'S HOSPITAL   (Canada)

Author keywords

Arteriovenous malformations; Children; Genetics; Hereditary hemorrhagic telangiectasia; HHT; Liver; Rendu Osler Weber; Visceral

Indexed keywords

ACTIVIN RECEPTOR LIKE KINASE 1; ANTIBIOTIC AGENT; INOTROPIC AGENT; IODINATED POPPYSEED OIL;

ACUTE KIDNEY FAILURE; ALK1 GENE; ANGIOGRAPHY; ARTERY PERFORATION; ARTICLE; ARTIFICIAL EMBOLISM; BLOOD CLOTTING DISORDER; CANADA; CARDIOMEGALY; CASE REPORT; CAUSE OF DEATH; CONGESTIVE HEART FAILURE; DOPPLER ECHOGRAPHY; ECHOCARDIOGRAPHY; FEMALE; GENE; GENETIC SCREENING; HEPATIC ARTERIOVENOUS MALFORMATION; HETEROZYGOSITY; HUMAN; HUMAN CELL; HYPOXEMIA; ILEOSTOMY; ILEUM DISEASE; ILEUM RESECTION; INFANT; LACTIC ACIDOSIS; LIVER DISEASE; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; OUTCOME ASSESSMENT; PEDIATRICS; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; RESPIRATORY TRACT DISEASE; SEPSIS; SURVIVAL; SYMPTOMATOLOGY; THROMBOCYTOPENIA;

ANGIOGRAPHY; DIAGNOSIS, DIFFERENTIAL; EMBOLIZATION, THERAPEUTIC; FEMALE; FOLLOW-UP STUDIES; HUMANS; INFANT, NEWBORN; LIVER; LIVER DISEASES; MALE; TELANGIECTASIA, HEREDITARY HEMORRHAGIC; VASCULAR MALFORMATIONS;

EID: 79957921000     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2010-2366     Document Type: Article

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