Monozygotic twins with identical premature timing of acne onset: A Case report

Author:

Tan Amanda S. H.1ORCID,Chia Shi Yun2ORCID,Lim Jiin Ying3ORCID,Chan Daniel4

Affiliation:

1. Department of Paediatrics KK Women's and Children's Hospital Singapore Singapore

2. Department of Dermatology KK Women's and Children's Hospital Singapore Singapore

3. Genetic Service, Department of Paediatrics KK Women's and Children's Hospital Singapore Singapore

4. Endocrinology Service, Department of Paediatrics KK Women's and Children's Hospital Singapore Singapore

Abstract

AbstractAcne vulgaris, a common dermatological condition that affects most adolescents and young adults, can indicate an underlying pathology if present prematurely in mid‐childhood. Premature acne can be caused by premature adrenarche secondary to non‐classical congenital adrenal hyperplasia (NC‐CAH), a condition arising from 21‐hydroxylase deficiency. This report describes a pair of monozygotic twin brothers with identical premature onset of acne, who were found to have an identical homozygous mutation in the promoter region of the CYP21A2 gene. While it is widely known that NCCAH is associated with genetic changes, the drive behind onset of adrenarche are widely unknown. As such, this report provokes thoughts on whether adrenarche could be influenced by adrenal genetic polymorphisms.

Publisher

Wiley

Subject

Dermatology

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