Article
GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome.
American journal of medical genetics. Part A - 1 Mar 2026
Meiss Lauren N, Karam Amanda V, Shalen Julia, Tunkel David E, Yi Belina Y, Guthrie Kelsey S, Kudalkar Emily M, Patrick Anna E, Rasmussen Sonja A
Abstract excerpt
Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10-year-old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA). The patient presented for genetics evaluation with bilateral sensorineural hearing loss, oligoarticular JIA, and a renal cyst. Trio-based...
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