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Colombia Médica

On-line version ISSN 1657-9534

Abstract

MATALLANA-RHOADES, Audrey Mary et al. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X. Colomb. Med. [online]. 2016, vol.47, n.3, pp.172-175. ISSN 1657-9534.

Case Description:

It is presented the phenotype of a new compound heterozygous mutation of the genes R384X and Q356X encoding the enzyme of 11-beta-hydroxylase

Clinical Findings:

Severe virilization, peripheral hypertension, and early puberty.

Treatment and Outcome:

Managed with hormone replacement therapy (corticosteroid) and antihypertensive therapy (beta-blocker), resulting in the control of physical changes and levels of arterial tension.

Clinical Relevance:

According to the phenotypic characteristics of the patient, it is inferred that the R384X mutation carries an additional burden on the Q356X mutation, with the latter previously described as a cause of 11-beta-hydroxylase deficiency. The description of a new genotype, as in this case, expands the understanding of the hereditary burden and deciphers the various factors that lead to this pathology as well as the other forms of congenital adrenal hyperplasia (CAH), presenting with a broad spectrum of clinical presentations. This study highlights the importance of a complete description of the patient's CAH genetic profile as well as their parents' genetic profile.

Keywords : Adrenal hyperplasia congenital; hyperplasia adrenal glands; mutation; adrenocorticotropic hormone, Virilism, 11-beta-hydroxylase deficiency.

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