Clinical and Molecular Spectrum of Somatic Mosaicism in Androgen Insensitivity Syndrome
- 1 December 1999
- journal article
- case report
- Published by Springer Nature in Pediatric Research
- Vol. 46 (6) , 684
- https://doi.org/10.1203/00006450-199912000-00009
Abstract
We recently found that postzygotic de novo mutations occur at the expected high rate of an X-linked recessive mutation in androgen insensitivity syndrome. The resulting somatic mosaicism can be an important molecular determinant of in vivo androgen action caused by expression of the wild-type androgen receptor (AR). However, the clinical relevance of this previously underestimated genetic condition in androgen insensitivity syndrome has not been investigated in detail as yet. Here, we present the clinical and molecular spectrum of somatic mosaicism considering all five patients with mosaic androgen insensitivity syndrome, whom we have identified since 1993: Patient 1 (predominantly female, clitoromegaly), 172 TTA(Leu)/TGA(Stop); patient 2 (ambiguous), 596 GCC(Ala)/ACC(Thr); patient 3 (ambiguous), 733 CAG(Gln)/ CAT(His); patient 4 (completely female), 774 CGC(Arg)/TGC (Cys); and patient 5 (ambiguous), 866 GTG(Val)/ATG(Met). Serum sex hormone binding globulin response to stanozolol, usually correlating well with in vivo AR function, was inconclusive for assessment of the phenotypes in all tested mosaic individuals. An unexpectedly strong virilization occurred in patients 1, 3, and 5 compared with phenotypes as published with corresponding inherited mutations and compared with the markedly impaired transactivation caused by the mutant ARs in cotransfection experiments. Only the prepubertal virilization of patients 2 and 4 matched appropriately with transactivation studies (patient 4) or the literature (patients 2 and 4). However, partial pubertal virilization in patient 4 caused by increasing serum androgens and subsequent activation of the wild-type AR could not be excluded. We conclude that somatic mosaicism is of particular clinical relevance in androgen insensitivity syndrome. The possibility of functionally relevant expression of the wild-type AR needs to be considered in all mosaic individuals, and treatment should be adjusted accordingly.Keywords
This publication has 23 references indexed in Scilit:
- Inherited and de novo androgen receptor gene mutations: Investigation of single-case familiesThe Journal of Pediatrics, 1998
- Mosaicism due to a Somatic Mutation of the Androgen Receptor Gene Determines Phenotype in Androgen Insensitivity SyndromeJournal of Clinical Endocrinology & Metabolism, 1997
- Phenotypic diversity in siblings with partial androgen insensitivity syndromeArchives of Disease in Childhood, 1997
- Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndromeThe Journal of Steroid Biochemistry and Molecular Biology, 1997
- Molecular basis of androgen insensitivityThe Journal of Steroid Biochemistry and Molecular Biology, 1996
- Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor geneJournal of Clinical Endocrinology & Metabolism, 1996
- Functional Analysis of Six Androgen Receptor Mutations Identified in Patients with Partial Androgen Insensitivity SyndromeHuman Molecular Genetics, 1996
- Detection of point mutations in the androgen receptor gene using non-isotopic single strand conformation polymorphism analysisHuman Molecular Genetics, 1994
- 8 Androgen insensitivity syndromeBailliere's Clinical Endocrinology and Metabolism, 1994
- Mutations of androgen receptor gene in androgen insensitivity syndromesThe Journal of Steroid Biochemistry and Molecular Biology, 1993