3-Beta-Hydroxysteroid Dehydrogenase Deficiency

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/3-beta-hydroxysteroid-dehydrogenase-deficiency

3-beta (β)-hydroxysteroid dehydrogenase (HSD) deficiency is an inherited disorder that affects hormone-producing glands including the gonads (ovaries in females and testes in males) and the adrenal glands. The gonads direct sexual development before birth and during puberty. The adrenal glands, which are located on top of the kidneys, regulate the production of certain hormones and control salt levels in the body. People with 3β-HSD deficiency lack many of the hormones that are made in these glands. 3β-HSD deficiency is one of a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development and maturation.

genetic conditions

1. Introduction

There are three types of 3β-HSD deficiency: the salt-wasting, non-salt-wasting, and non-classic types. In the salt-wasting type, hormone production is extremely low. Individuals with this type lose large amounts of sodium in their urine, which can be life-threatening. Individuals affected with the salt-wasting type are usually diagnosed soon after birth due to complications related to a lack of salt reabsorption, including dehydration, poor feeding, and vomiting. People with the non-salt-wasting type of 3β-HSD deficiency produce enough hormone to allow sodium reabsorption in the kidneys. Individuals with the non-classic type have the mildest symptoms and do not experience salt wasting.

In males with any type of 3β-HSD deficiency, problems with male sex hormones lead to abnormalities of the external genitalia. These abnormalities range from having the opening of the urethra on the underside of the penis (hypospadias) to having external genitalia that do not look clearly male or female (ambiguous genitalia). The severity of the genital abnormality does not consistently depend on the type of the condition. Because of the hormone dysfunction in the testes, males with 3β-HSD deficiency are frequently unable to have biological children (infertile).

Females with 3β-HSD deficiency may have slight abnormalities of the external genitalia at birth. Females affected with the non-salt-wasting or non-classic types are typically not diagnosed until mid-childhood or puberty, when they may experience irregular menstruation, premature pubic hair growth, and excessive body hair growth (hirsutism). Females with 3β-HSD deficiency have difficulty conceiving a child (impaired fertility).

2. Frequency

The exact prevalence of 3β-HSD deficiency is unknown. At least 60 affected individuals have been reported.

3. Causes

Mutations in the HSD3B2 gene cause 3β-HSD deficiency. The HSD3B2 gene provides instructions for making the 3β-HSD enzyme. This enzyme is found in the gonads and adrenal glands. The 3β-HSD enzyme is involved in the production of many hormones, including cortisol, aldosterone, androgens, and estrogen. Cortisol has numerous functions such as maintaining energy and blood sugar levels, protecting the body from stress, and suppressing inflammation. Aldosterone is sometimes called the salt-retaining hormone because it regulates the amount of salt retained by the kidney. The retention of salt affects fluid levels and blood pressure. Androgens and estrogen are essential for normal sexual development and reproduction.

3β-HSD deficiency is caused by a deficiency (shortage) of the 3β-HSD enzyme. The amount of functional 3β-HSD enzyme determines whether a person will have the salt-wasting or non-salt-wasting type of the disorder. Individuals with the salt-wasting type have HSD3B2 gene mutations that result in the production of very little or no enzyme. People with the non-salt-wasting type of this condition have HSD3B2 gene mutations that allow the production of some functional enzyme, although in reduced amounts.

4. Inheritance

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

5. Other Names for This Condition

3 beta-HSD deficiency
3 beta-ol dehydrogenase deficiency
3-beta–hydroxysteroid dehydrogenase deficiency
3b-hydroxysteroid dehydrogenase deficiency
3β-HSD deficiency
3β-HSD deficiency congenital adrenal hyperplasia
3β-hydroxysteroid dehydrogenase deficiency
type II 3β-hydroxysteroid dehydrogenase deficiency

References

Lutfallah C, Wang W, Mason JI, Chang YT, Haider A, Rich B, Castro-Magana M,Copeland KC, David R, Pang S. Newly proposed hormonal criteria via genotypicproof for type II 3beta-hydroxysteroid dehydrogenase deficiency. J ClinEndocrinol Metab. 2002 Jun;87(6):2611-22.
Pan Y, Zhong S, Hu RM, Gong W. Mutation of 3β-hydroxysteroid dehydrogenase(3β-HSD) at the 3'-untranslated region is associated with adrenocorticalinsufficiency. Mol Med Rep. 2012 Dec;6(6):1305-8. doi: 10.3892/mmr.2012.1107.
Pang S, Carbunaru G, Haider A, Copeland KC, Chang YT, Lutfallah C, Mason JI.Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency canonly be identified by HSD3B2 genotype study and not by hormone test. ClinEndocrinol (Oxf). 2003 Mar;58(3):323-31.
Pang S, Wang W, Rich B, David R, Chang YT, Carbunaru G, Myers SE, Howie AF,Smillie KJ, Mason JI. A novel nonstop mutation in the stop codon and a novelmissense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD)gene causing, respectively, nonclassic and classic 3beta-HSD deficiencycongenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun;87(6):2556-63.
Pang S. Congenital adrenal hyperplasia owing to 3 beta-hydroxysteroiddehydrogenase deficiency. Endocrinol Metab Clin North Am. 2001 Mar;30(1):81-99,vi-vii. Review.
Simard J, Moisan AM, Morel Y. Congenital adrenal hyperplasia due to3beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase deficiency. Semin Reprod Med. 2002 Aug;20(3):255-76. Review.
Takasawa K, Ono M, Hijikata A, Matsubara Y, Katsumata N, Takagi M, Morio T,Ohara O, Kashimada K, Mizutani S. Two novel HSD3B2 missense mutations withdiverse residual enzymatic activities for Δ5-steroids. Clin Endocrinol (Oxf).2014 Jun;80(6):782-9. doi: 10.1111/cen.12394.
Welzel M, Wüstemann N, Simic-Schleicher G, Dörr HG, Schulze E, Shaikh G,Clayton P, Grötzinger J, Holterhus PM, Riepe FG. Carboxyl-terminal mutations in3beta-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenitaladrenal hyperplasia. J Clin Endocrinol Metab. 2008 Apr;93(4):1418-25. doi:10.1210/jc.2007-1874.

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Subjects: Genetics & Heredity

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Catherine Yang

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Entry Collection: MedlinePlus

Update Date: 23 Dec 2020

Table of Contents

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1. Introduction

2. Frequency

3. Causes

4. Inheritance

5. Other Names for This Condition

References

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1. Introduction

2. Frequency

3. Causes

3.1. The gene associated with 3-beta-hydroxysteroid dehydrogenase deficiency

4. Inheritance

5. Other Names for This Condition

References