Congenital Lipoid Adrenal Hyperplasia Developed in a Brother and Sister / 대한주산의학회잡지
Korean Journal of Perinatology
;
: 191-195, 2010.
Article
in Korean
| WPRIM
| ID: wpr-6944
ABSTRACT
Congenital lipoid adrenal hyperplasia (lipoid CAH) is an autosomal recessive disorder characterized by severe adrenal insufficiency. Clinical findings of patients are salt loss, hypoglycemia, pigmentation and male sex reversal. And also the baby with inadequate treatment may result in sudden death from adrenal crisis. We report the case of lipoid CAH developed in siblings with a brief review of associated literatures.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pigmentation
/
Adrenal Insufficiency
/
Death, Sudden
/
Siblings
/
Hyperplasia
/
Hypoglycemia
Limits:
Humans
/
Male
Language:
Korean
Journal:
Korean Journal of Perinatology
Year:
2010
Type:
Article
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