11β-hydroxylase deficiency history and symptoms: Difference between revisions
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* [[Family history]] of 11β-hydroxylase deficiency | * [[Family history]] of 11β-hydroxylase deficiency | ||
==Common Symptoms== | ==Common Symptoms== | ||
In classic form of 11β-hydroxylase deficiency, male and female and children clinical findings are as follows: | |||
=== Female === | |||
* [[Ambiguous genitalia]] | |||
* [[Clitoromegaly]] | |||
* [[Labial fusion]] | |||
* [[Hirsutism]] | |||
* [[Menstrual irregularities]] | |||
* Aggressive behavior | |||
=== Male === | |||
* Increased penile size in [[newborns]] | |||
* [[Acne]] | |||
=== Children === | |||
Children who are not diagnosed at birth, may present with: | |||
* [[Premature]] [[adrenarche]] | |||
* Adult [[body odor]] | |||
* [[Axillary]] and [[pubic hair]] development | |||
* Faster growth and [[bone age]] in [[premature]] [[adrenarche]] | |||
* [[Hypertension]] in children or adolescents, occurs in approximately two-thirds of patients<ref name="pmid7988480">{{cite journal |vauthors=White PC, Curnow KM, Pascoe L |title=Disorders of steroid 11 beta-hydroxylase isozymes |journal=Endocr. Rev. |volume=15 |issue=4 |pages=421–38 |year=1994 |pmid=7988480 |doi=10.1210/edrv-15-4-421 |url=}}</ref><ref name="pmid2984117">{{cite journal |vauthors=de Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, Lombardi G |title=Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension |journal=Hypertension |volume=7 |issue=2 |pages=204–10 |year=1985 |pmid=2984117 |doi= |url=}}</ref><ref name="pmid3011843">{{cite journal |vauthors=Hochberg Z, Benderly A, Kahana L, Zadik Z |title=Requirement of mineralocorticoid in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency |journal=J. Clin. Endocrinol. Metab. |volume=63 |issue=1 |pages=36–40 |year=1986 |pmid=3011843 |doi=10.1210/jcem-63-1-36 |url=}}</ref><ref name="pmid6607265">{{cite journal |vauthors=Zadik Z, Kahana L, Kaufman H, Benderli A, Hochberg Z |title=Salt loss in hypertensive form of congenital adrenal hyperplasia (11-beta-hydroxylase deficiency) |journal=J. Clin. Endocrinol. Metab. |volume=58 |issue=2 |pages=384–7 |year=1984 |pmid=6607265 |doi=10.1210/jcem-58-2-384 |url=}}</ref> | |||
==Less Common Symptoms== | ==Less Common Symptoms== | ||
| Line 37: | Line 37: | ||
=== Male === | === Male === | ||
* [[Testicular masses]] due to [[testicular]] [[Adrenal tumor|adrenal rest tumors]]; these tumors caused by high level of ACTH | * [[Testicular masses]] due to [[testicular]] [[Adrenal tumor|adrenal rest tumors]]; these [[tumors]] caused by high level of ACTH | ||
* [[Gonadal]] dysfunction as a result of testicular [[Adrenal tumor|adrenal rest tumors]] | * [[Gonadal]] dysfunction as a result of testicular [[Adrenal tumor|adrenal rest tumors]] | ||
* [[Infertility]] due to [[seminiferous tubule]] obstruction | * [[Infertility]] due to [[seminiferous tubule]] obstruction | ||
Latest revision as of 19:39, 18 October 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Mehrian Jafarizade, M.D [2]
Overview
Symptoms of 11β-hydroxylase deficiency include female patients with ambiguous genitalia, clitoromegaly, labial fusion, hirsutism, menstrual irregularities, aggressive behavior; male patients present with increased penile size in newborns, acne. Children who are not diagnosed at birth, may present with premature adrenarche, adult body odor, axillary and pubic hair development, faster growth and bone age in premature adrenarche.
History
- History of pseudo-precocious puberty
- Family history of 11β-hydroxylase deficiency
Common Symptoms
In classic form of 11β-hydroxylase deficiency, male and female and children clinical findings are as follows:
Female
- Ambiguous genitalia
- Clitoromegaly
- Labial fusion
- Hirsutism
- Menstrual irregularities
- Aggressive behavior
Male
Children
Children who are not diagnosed at birth, may present with:
- Premature adrenarche
- Adult body odor
- Axillary and pubic hair development
- Faster growth and bone age in premature adrenarche
- Hypertension in children or adolescents, occurs in approximately two-thirds of patients[1][2][3][4]
Less Common Symptoms
Female
- Cognitive function disturbance such as IQ impairment
- Male-typical cognitive pattern (better performance on spatial tasks, worse performance on verbal tasks)
Male
- Testicular masses due to testicular adrenal rest tumors; these tumors caused by high level of ACTH
- Gonadal dysfunction as a result of testicular adrenal rest tumors
- Infertility due to seminiferous tubule obstruction
Non-classic type is a rare and mild disease than the classic type.
References
- ↑ White PC, Curnow KM, Pascoe L (1994). "Disorders of steroid 11 beta-hydroxylase isozymes". Endocr. Rev. 15 (4): 421–38. doi:10.1210/edrv-15-4-421. PMID 7988480.
- ↑ de Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, Lombardi G (1985). "Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension". Hypertension. 7 (2): 204–10. PMID 2984117.
- ↑ Hochberg Z, Benderly A, Kahana L, Zadik Z (1986). "Requirement of mineralocorticoid in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency". J. Clin. Endocrinol. Metab. 63 (1): 36–40. doi:10.1210/jcem-63-1-36. PMID 3011843.
- ↑ Zadik Z, Kahana L, Kaufman H, Benderli A, Hochberg Z (1984). "Salt loss in hypertensive form of congenital adrenal hyperplasia (11-beta-hydroxylase deficiency)". J. Clin. Endocrinol. Metab. 58 (2): 384–7. doi:10.1210/jcem-58-2-384. PMID 6607265.