Definition

Homozygous or compound heterozygous mutations in the HSD3B2 gene impair the 3β-hydroxysteroid dehydrogenase type 2 enzyme, which functions in the synthesis of cortisol, aldosterone and gonadal steroids; the result is severe deficiency. In the classic form, male infants may show ambiguous genitalia due to inadequate virilization, while female infants may show mild virilization; some mutations lead to a salt-wasting crisis.

Gene/region examined

HSD3B2 - Exon 1, HSD3B2 - Exon 2, HSD3B2 - Exon 3, HSD3B2 - Exon 4

Method

Sequence analysis

Accepted sample types

EDTA blood, AF, CVS

Inheritance

Hereditary, autosomal recessive (AR).

Related Tests

Inheritance Patterns

Describes how a genetic condition is passed on within a family. There are five main patterns

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Carrier (Heterozygous / Homozygous)

Why it matters: In autosomal recessive inheritance, when each parent is a carrier (while both appear healthy), the chance of their child being born with the disease is 25% in each

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VUS (Variant of Uncertain Significance)

This is the situation where the test has detected a change in the DNA, but the role of this change in the development of disease is unconfirmed.

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How to Read a Genetic Test Result (Positive / Negative / VUS)

A genetic test result falls into three main categories

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Types of Genetic Tests

A genetic test is a type of medical test that detects changes in genes, chromosomes or proteins. Today there are more than 77,000 genetic tests available.

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