Congenital Adrenal Hyperplasia — High-Yield Exam Topic

Congenital adrenal hyperplasia (CAH) is a group of inherited disorders of adrenal steroid synthesis, most commonly caused by 21-hydroxylase deficiency. It can present with virilization, salt wasting, dehydration, hypotension, or precocious androgen effects, depending on the enzyme defect and severity. For exam questions, the key is to recognize the clinical pattern, blood pressure, electrolytes, and characteristic hormone abnormality to identify the enzyme defect quickly.

Key concept

Congenital adrenal hyperplasia (CAH) is a group of autosomal-recessive disorders of adrenal steroid synthesis. Impaired cortisol synthesis causes ↑ ACTH, adrenal hyperplasia and accumulation of steroid precursors. The clinical picture depends on the enzyme affected and the severity of the defect. 21-hydroxylase deficiency accounts for >90% of CAH cases and is the most important form for pediatric exams.

21-Hydroxylase deficiency — most important

21-hydroxylase deficiency → ↓ cortisol + ↑ adrenal androgens

In the salt-wasting form, there is also significant ↓ aldosterone, resulting in:

  • Hyponatremia
  • Hyperkalemia
  • Dehydration
  • Hypotension
  • Adrenal crisis

The characteristic biochemical marker is markedly elevated 17-hydroxyprogesterone (17-OHP). Newborn screening for 21-hydroxylase deficiency uses 17-OHP.

Clinical presentations

46,XX newborn:

  • Virilized/ambiguous external genitalia
  • May have clitoromegaly and labioscrotal fusion

46,XY newborn:

  • External genitalia may appear normal at birth
  • Salt-wasting crisis may subsequently reveal the diagnosis

Later childhood/adolescence:

  • Premature adrenarche/pubarche
  • Rapid growth
  • Advanced bone age
  • Acne, hirsutism or menstrual irregularity in females

Three phenotypes of 21-hydroxylase deficiency

Salt-wasting classic CAH
→ severe enzyme deficiency
→ ↓ cortisol + ↓ aldosterone + ↑ androgens
→ salt wasting and adrenal crisis

Simple-virilizing classic CAH
→ ↓ cortisol + ↑ androgens
→ sufficient mineralocorticoid activity to avoid clinically significant salt wasting

Non-classic CAH
→ milder enzyme deficiency
→ later androgen excess
→ usually no salt-wasting crisis
→ may present with premature adrenarche, acne, hirsutism or menstrual irregularity.

In a boy with non-classic CAH

Because residual 21-hydroxylase activity is present, aldosterone production is generally sufficient, so he does not present with the classic salt-wasting crisis. Instead, the excess adrenal androgens may cause:

  • Premature pubic/axillary hair
  • Rapid linear growth
  • Advanced bone age
  • Early penile enlargement
  • Early beard/virilization
  • Precocious puberty or precocious pubertal development

Other enzyme defects — very high yield

Enzyme defectAndrogensMineralocorticoid effectBPClassic clue
21-hydroxylaseVirilization + salt wasting
11β-hydroxylase↑ DOCVirilization + hypertension
17α-hydroxylase↑ DOCHypertension + low sex steroids

Memory aid

21 → salt loss + androgens ↑

11 → hypertension + androgens ↑

17 → hypertension + androgens ↓

How to Approach a CAH MCQ

1. Look for androgen excess

Ambiguous genitalia/virilization in a newborn girl → think CAH, particularly 21-hydroxylase deficiency.

2. Look for salt wasting

Vomiting + dehydration + hypotension + hyponatremia + hyperkalemia

→ strongly suggests salt-wasting 21-hydroxylase deficiency.

3. Check the blood pressure

Hypotension/salt wasting → 21-hydroxylase

Hypertension + virilization → 11β-hydroxylase

Hypertension + undervirilization/sexual infantilism → 17α-hydroxylase

4. Look at the hormone

↑ 17-OHP → 21-hydroxylase deficiency

For symptomatic patients beyond infancy, an early-morning 17-OHP is recommended. If the result is borderline, an ACTH (cosyntropin) stimulation test with a broader adrenal steroid profile can help distinguish 21-hydroxylase deficiency from other enzyme defects.

5. If the question asks about treatment

Classic CAH → glucocorticoid replacement with hydrocortisone.

Salt-wasting disease additionally requires mineralocorticoid replacement (fludrocortisone) and, particularly in infancy, sodium supplementation. During adrenal crisis, treatment requires urgent parenteral hydrocortisone and appropriate fluid/electrolyte and glucose management

Very useful MCQ pattern

Boy aged 6–8 years + pubic hair + penile enlargement + rapid growth + advanced bone age + no salt wasting → think CAH, particularly 21-hydroxylase deficiency.

Quick Approach

Virilization + salt wasting + hypotension → 21-hydroxylase deficiency

Virilization + hypertension → 11β-hydroxylase deficiency

Hypertension + low sex steroids → 17α-hydroxylase deficiency

↑ 17-OHP → 21-hydroxylase deficiency

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