WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion. Issue 6 (11th April 2017)

• Record Type: Journal Article
• Authors: Huynh, Minh Tuan; Boudry‐Labis, Elise; Duban, Bénédicte; Andrieux, Joris; Tran, Cong Toai; Tampere, Heidi; Ceraso, Delphine; Manouvrier, Sylvie; Tachdjian, Gérard; Roche‐Lestienne, Catherine; Vincent‐Delorme, Catherine
• Is Part Of: American journal of medical genetics. Volume 173:Issue 6(2017)
• Page Start: 1690
• Page End: 1693
• Publication Date: 2017-04-11
• Subjects: congenital hypothyroidism -- mosaic 11p13 deletion -- thyroid ectopia -- WAGR syndrome; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.38206
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract : Wilm's tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome, a rare genetic disorder, is caused by the loss of 11p13 region including PAX6 and WT1 . We report novel findings in a 28‐month‐old boy with aniridia, Wilm's tumor, congenital hypothyroidism, and sublingual thyroid ectopia. He was found to have a mosaic 5.28 Mb interstitial deletion of chromosome 11p13 deleting PAX6 and WT1 . In order to clarify the mechanism underlying his thyroid dysgenesis, sequence analysis of candidate thyroid developmental genes was performed. We identified a FOXE1 : c.532_537delGCCGCC p.(Ala178_Ala179del) variant that predisposes to thyroid ectopia. Taken together, this is the first report of mosaic 11p13 deletion in association with thyroid dysgenesis. We also propose a model of complex interactions of different genetic variants for this particular phenotype in the present patient.