Congenital adrenal hyperplasia

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Congenital adrenal hyperplasia (CAH, formerly adrenogenital syndrome ) is a group of autosomal recessive inherited steroid hormone synthesis disorders caused by the absence of any of the five essential enzymes. Enzymatic block leads to a deficiency of part of the spectrum of steroid hormones and an excess of another group of hormones due to overproduction of ACTH in the release of feedback. The clinical picture is specific for each type of enzymatic defect.  The most common is 21-hydroxylase deficiency ( CYP21 gene ). Failure to recognize and treat severe forms of CAH leads to salt wasting syndrome, hyponatremia, hyperkalemia, dehydration and hypotension.

Enzymes involved in the production of steroid adrenal cortex hormones: SCC / 20,22-desmolase, 17-alpha-hydroxylase / 17,20-desmolase, 21-alpha-hydroxylase, 11-beta-hydroxylase, aldosterone synthetase .

Adrenal function and its disorders[edit | edit source]

Steroidogeneze.

The adrenal medulla and cortex are 2 histologically and functionally different parts, which are derived from different germinal tissues in embryonic development.

Adrenal medulla
  • comes from ectoderm , developmentally cleaves from nervous tissue; functionally it is close to the sympathetic nerve ganglia;
  • produces catecholamines : adrenaline, noradrenaline;
  • Hyperfunctional tumor - pheochromocytoma .
Adrenal cortex

Adrenal disorders in children[edit | edit source]

Osa hypotalamus (CRH) - hypofýza (ACTH) - kůra nadledvin (kortizol, androgeny).

Congenital adrenal hyperplasia (CAH)
  • a group of congenital enzymatic disorders of steroidogenesis , which lead to a deficiency of a part of the spectrum of steroid hormones and due to feedback through ACTH to overproduction of other steroids.
Adrenal insufficiency
  • reduced ability to synthesize and secrete steroid hormones;
  • congenital (acquired) or acquired causes (adrenal bleeding, infections, autoimmune diseases - Addison's disease ).
Overproduction of adrenal hormones

21-hydroxylase deficiency[edit | edit source]

Teoretická 3D struktura 21-hydroxylázy.

  • 95% of CAH patients have 21-hydroxylase deficiency;
  • in the Czech Republic frequency 1:10 000;
  • severe secretion of cortisol and aldosterone , ACTH output increases → production of adrenal metabolites with androgenic activity;
  • clinical manifestations depend on the type of gene mutation that determines the residual activity of the enzyme:
  1. Classical form
    • with salt-wasting
        • zero 21-hydroxylase activity
        • boys: salt crisis in the 2nd to 4th week of life (hyponatremia, hyperkalemia, hypoglycemia), severe condition, sudden death
        • girls: virilization of the external genitalia (high levels of androgens in utero , evaluation according to the Prader scale), salt crisis, severe condition, sudden death
    • simple virilising
  2. late-onset
        • 20-50% 21-hydroxylase activity
        • boys: clinically dumb
        • girls: hirsutism , cycle disorders, infertility.
Laboratory diagnostics
  • elevated 17-hydroxyprogesterone (17-OHP);
  • low cortisol, high ACTH;
  • synactene test;
  • full-area neonatal laboratory screening (17-OHP from a dry drop) - captures the classic form with a salt disorder.
Therapy
  • acute condition: hydrocortisone 50–100 mg iv, parenteral rehydration, ionogram correlation, prevention of hypoglycemia;
  • long-term treatment of the classic form: substitution of hydrocortisone and mineralocorticoid → suppression of ACTH overproduction;
  • in girls with virilization of the external genitalia, surgical correction;
  • with a positive family history - prenatal treatment of the fetus with dexamethasone from the 8th week of pregnancy, in female fetuses until delivery (prevention of virilization).

17α-hydroxylase deficiency[edit | edit source]

Přehled syntézy steroidních hormonů.

  • the adrenal gland produces only mineralocorticoid precursors, lacking cortisol, androgens and estrogens ;
  • boys: insufficient virilization of the external genitalia in utero, with a complete block of the girl's external genitalia with a blind-ended vagina, testes intra-abdominally;
  • lack of pubertal development;
  • hypokalaemia, borderline hypernatraemia, hypertension (due to increased levels of mineralocorticoids);
  • in stressful situations, cortisol deficiency shock;
  • diagnosis mostly on the basis of accidentally detected hypertension or for incoming adolescence .

11-hydroxylase deficiency[edit | edit source]

It causes insufficient production of cortisol and aldosterone , increased production of androgens and 11-deoxycortisol and 11-deoxycorticosterone, which have mineralocorticoid effects. Virilization and the development of mineralocorticoid hypertension occur . The therapy is based on the administration of glucocorticoids (without mineralocorticoids).

3βHSD deficiency[edit | edit source]

This is a very rare disorder in which cortisol and aldosterone are not produced enough. The resulting androgens are weak and therefore there is only slight virilization.

Adrenogenital syndrome[edit | edit source]

Adrenogenital syndrome from estrogen overproduction[edit | edit source]

  • This form is very rare. It is always caused by a tumor of the adrenal cortex ( cancer , adenoma). It most commonly occurs in adult men who develop gynecomastia , testicular atrophy, and impotence . The affected boy develops pseudopubertas praecox heterosexualis before puberty .

Adrenogenital androgenic syndrome[edit | edit source]

Post-mortem dětské nadledviny s CAH

  • Acquired - the cause is a tumor of the adrenal cortex ( carcinomas , adenomas ). It occurs most often in children. Pseudopubertas praecox isosexualis develops in affected boys before puberty, and pseudopubertas praecox heterosexualis develops in affected girls before puberty . In adult women, masculinization (virilization), hirsutism (excessive hair loss in women caused by endocrine disorders), clitoral hypertrophy, voice thickening and amenorrhea (lack of menstruation) occur.
  • Congenital (or congenital adrenal hyperplasia , CAH) - is caused by a deficiency of an enzyme that metabolizes steroids . Most often, in about 90% of cases, it is a deficiency of 21-hydroxylase (= P450 C21 ). The second most common is 11β-hydroxylase deficiency. Lack of other enzymes (3β-hydroxysteroid dehydrogenases - 3βHSD, 17/17, 20 lyases, enzymes involved in SSC - StAR and P450 SSC , P450-oxidoreductase) is rare.

Due to the absence of one of the previous enzymes, hypocortisolism (reduced cortisol production ) develops, which causes increased ACTH production in the pituitary gland (the pituitary gland wants to increase cortisol levels). This leads to bilateral hyperplasia of the adrenal cortex (therefore in this case the adrenogenital syndrome is otherwise called congenital adrenal hyperplasia ). More ACTH causes more steroids that are not affected by enzyme deficiency.

Deficiencies of 21-hydroxylase, 11β-hydroxylase and 3βHSD (basic forms of CAH) distinguish between classical and non-classical forms . Classical forms have a more difficult course and appear after birth or in childhood. Non-classical forms are less severe, may be asymptomatic, or may manifest during adolescence or adulthood.

Cortisol deficiency can cause an adrenal crisis .

Links[edit | edit source]

related articles[edit | edit source]

Reference[edit | edit source]

  1. WILSON, TA, et al. Congenital Adrenal Hyperplasia  [online]. Medscape, © 2012. [feeling. 2012-07-10]. < https://emedicine.medscape.com/article/919218-overview >.
  2. ↑Jump up to:a b c d LEBL, J, J JANDA and P POHUNEK, et al. Clinical pediatrics. 1st edition. Galén, 2012. 698 pp. 196-200. ISBN 978-80-7262-772-1 .

Reference[edit | edit source]

    • POVÝŠIL, Ctibor, et al. Special pathology. 2nd edition. Prague: Galén, 207. 430 pp. 383.  ISBN 978-80-7262-494-2 .
    • MURRAY, Robert K, et al. Harper's Biochemistry. 4th edition. Prague: H + H, 2002. 872 pp. 560-561. ISBN 80-7319-013-3 .
    • CZECH, Richard, et al. Internal. 1st edition. Prague: TRITON, 2010. 855 pp. 353-354. ISBN 978-80-7387423-0 .
    • KUMAR, Vinay, Ramzi S COTRAN and Stanley L ROBBINS. Robbins Basic Pathology. 7th edition. Saunders, 2003. 873 pp. 746-748. ISBN 978-1-4160-2534-4 .

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