Laurence-Moon-Bardet-Biedl syndrome.
Article
in English
| IMSEAR
| ID: sea-46035
ABSTRACT
Laurence-Moon-Bardet-Biedl syndrome is a rare, genetically heterogeneous, autosomal recessive inherited disorder with wide variability in expression. We report a case of Laurence-Moon-Bardet-Biedl syndrome with typical phenotype in conjunction with nonalcoholic steatohepatitis. The diagnosis had been missed until the patient presented at our hospital.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Humans
/
Male
/
Child
/
Follow-Up Studies
/
Bardet-Biedl Syndrome
/
Diagnosis, Differential
/
Diet, Carbohydrate-Restricted
/
Exercise Therapy
/
Fatty Liver
Type of study:
Diagnostic study
/
Observational study
/
Prognostic study
/
Risk factors
Language:
English
Year:
2008
Type:
Article
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