Two Cases of ARC (Arthrogryposis, renal dysfunction and cholestasis) Syndrome / 대한소아소화기영양학회지
Korean Journal of Pediatric Gastroenterology and Nutrition
;
: 110-115, 2000.
Article
in Korean
| WPRIM
| ID: wpr-167713
ABSTRACT
ARC (arthrogryposis multiplex congrnita, renal dysfunction and cholestasis) syndrome was first described by Lutz-Richner and Landolt in 1973 and after then similar cases were scarcely reported worldwide. There's no reported case in Korea. It was first suggested that ARC syndrome was inherited by X-linked recessive trait but now it was thought to be inherited by autosomal recessive trait also. Most parents were consanguineous but some unconsanuineous parents were also reported. We report on 1 male and 1 female infant who had ARC syndrome from 2 unrelated families. They were born from unconsanguineous parents.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Parents
/
Arthrogryposis
/
Cholestasis
/
Korea
Limits:
Female
/
Humans
/
Infant
/
Male
Country/Region as subject:
Asia
Language:
Korean
Journal:
Korean Journal of Pediatric Gastroenterology and Nutrition
Year:
2000
Type:
Article
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