Alstrom syndrome with hepatic dysfunction: Report of one case

Acta Paediatrica Taiwanica

Volumn 41, Issue 5, 2000, Pages 270-272

  Chang, K W ^a   Hou, J W ^a   Lin, S J ^a   Kong, M S ^a  

^a CHANG GUNG CHILDREN S HOSPITAL   (Taiwan)

Author keywords

Alstrom syndrome; Hepatic dysfunction

Indexed keywords

ALANINE AMINOTRANSFERASE; LIVER ENZYME;

ACANTHOSIS NIGRICANS; ALSTROM SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DISEASE ASSOCIATION; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERGLYCEMIA; HYPERINSULINEMIA; LIVER DISEASE; MALE; OBESITY; PERCEPTION DEAFNESS; RETINOPATHY; SCHOOL CHILD; SYNDROME DELINEATION; TAIWAN;

ACANTHOSIS NIGRICANS; CHILD; HEARING LOSS, SENSORINEURAL; HUMANS; LIVER; MALE; OBESITY; RETINAL DISEASES; SYNDROME;

EID: 0033742330     PISSN: 00016578     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Genealogy, natural history, and phenotype of Alstrom syndrome in a large Acadian kindred and three additional families
2. Alstrom syndrome: Report of 22 cases and literature review
3. Refinement of genetic localization of the Alstrom syndrome on chromosome 2p12-13 by linkage analysis in a North African family
4. Natural history of Alstrom syndrome in early childhood: Onset with dilated cardiomyopathy
5. Hepatic dysfunction in Alstrom disease
6. Hepatic dysfunction in two sibs with Alstrom syndrome: Case report and review of the literature