Literature DB >> 16895568

[Acne infantum as presenting symptom of congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency].

Viola Harde1, Marina Müller, Wolfgang G Sippell, Thomas Schwarz, Regina Fölster-Holst.   

Abstract

Infantile acne is a rare condition which usually begins after the third month of life and appears mainly on the cheeks. Spontaneous healing typically occurs within 2 years. A 2-year-old boy developed acne infantum during the first days after birth; it failed to respond to topical treatment. Detailed physical examination and endocrinologic evaluation confirmed the presumed diagnosis of congenital adrenal hyperplasia (CAH), and showed it was caused by 11-beta-hydroxylase deficiency. CAH comprises a group of autosomal-recessively inherited disorders. These hereditary enzyme defects in steroid biosynthesis cause glucocorticoid deficiency and an overproduction of biosynthetic precursor steroids. Adrenal androgen biosynthesis is not impaired but shows a massive reactive overproduction due to the increased ACTH secretion within the up-regulated hypothalamo-pituitary-adrenal system. The characteristic features of CAH in male infants are demonstrated on the basis of this case report.

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Year:  2006        PMID: 16895568     DOI: 10.1111/j.1610-0387.2006.06016.x

Source DB:  PubMed          Journal:  J Dtsch Dermatol Ges        ISSN: 1610-0379            Impact factor:   5.584


  3 in total

1.  [Systemic retinoid therapy in severe acne infantum].

Authors:  M Hütten; J M Baron; H Ott
Journal:  Hautarzt       Date:  2008-06       Impact factor: 0.751

Review 2.  Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Authors:  Krupali Bulsari; Henrik Falhammar
Journal:  Endocrine       Date:  2016-12-07       Impact factor: 3.633

3.  Congenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child.

Authors:  Efat Khorasani; Rahim Vakili
Journal:  Iran J Med Sci       Date:  2016-01
  3 in total

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