Adrenal
Congenital Adrenal Hyperplasia
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Congenital Adrenal Hyperplasia
See Also
Adrenal Insufficiency
Steroid Hormone Pathway
Definition
Inherited
Adrenal Insufficiency
onset at birth
Pathophysiology
Autosomal Recessive
inheritance
Group of defective enzymes in
Cortisol Synthesis
Six different enzyme deficiencies possible
See
Steroid Hormone Pathway
21-Hydroxylase deficiency is most common (90%)
Types
Complete Enzyme Deficiency (Classic, Salt-losing)
Onset as newborn with adrenal crisis by 2 weeks old (as maternal
Cortisol
wanes)
Most common cause of
Ambiguous Genitalia
in females
Female genitalia are more significantly affected than male genitalia
Females are therefore typically diagnosed in newborn nursery (as opposed to boys who present later)
Partial Enzyme Deficiency (Simple virilizing)
Adrenal Insufficiency
occurs only as stress reaction
Causes
Androgen Excess
in later childhood
Precocious Puberty
Hirsutism
Acne Vulgaris
Symptoms
Presenting
Vomiting
Lethargy
Decreased oral intake
Signs
See
Adrenal Insufficiency
See
Ambiguous Genitalia
See
Precocious Puberty
Diagnosis
Classic (complete deficiency) type in newborns
17-Hydroxyprogesterone increased
Non-classic (Partial deficiency) type in children
17-Hydroxyprogesterone increased 1 hour post-
ACTH
Labs
Serum
Electrolyte
s
Hyponatremia
Hypochloremia
Hyperkalemia
Hypoglycemia
Adrenal labs
Low
Cortisol
Low
Aldosterone
High renin
Sex
Hormone
abnormalities depend on enzyme deficiency
Virilizing if 21-Hydroxylase or 11-Hydroxylase
Testosterone
increased in girls
Androstenedione
increased in girls and boys
Diagnostics
Electrocardiogram
(EKG)
Indicated for
Hyperkalemia
Management
Initial priorities
Rehydration with
Normal Saline
in small boluses (10 cc/kg)
Correct
Hypoglycemia
Hydrocortisone
IV
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