Alagille's Syndrome New Manifestations

Clinical Nuclear Medicine

Volumn 21, Issue 2, 1996, Pages 98-101

  Balich, Susan ^a   Jarboe, Gerald L ^a   Stevens, Jeffrey S ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEBROFENIN TC 99M;

ALAGILLE SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LIVER SCINTISCANNING; MALE; NEWBORN; OBSTRUCTIVE JAUNDICE; RADIOISOTOPE DISTRIBUTION;

ALAGILLE SYNDROME; CHOLESTASIS; GALLBLADDER; HEART; HUMANS; IMINO ACIDS; INFANT; LIVER; MALE; ORGANOTECHNETIUM COMPOUNDS; TIME FACTORS;

EID: 0030028002     PISSN: 03639762     EISSN: None     Source Type: Journal    
DOI: 10.1097/00003072-199602000-00003     Document Type: Article

References (4)

1. Kuni CC, Klingensmith WC: Atlas of Radionuclide Hepatobiliary Imaging. Boston, GK Hall, 1983, pp 210-211.
2. Aburano T, Yokoyama K, Takayama T, et al: Distinct hepatic retention of Tc-99m IDA in arteriohepatic dysplasia (Alagille Syndrome). Clin Nuc Med 14:874, 1989.
3. Alagille D, Odievre M, Gautier M, et al. Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental and sexual development, and cardiac murmur. J Pediatr 86:63, 1975.
4. Alagille D, Estrada A, Hadchouel M, et al. Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia: Review of 80 cases. J Pediatr 110:195, 1987.