@article{10.37349/eemd.2024.00009,
abstract = {Hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome is a rare genetic disorder caused by haploinsufficiency of the GATA3 gene. A very limited number of cases have been reported in the literature to date. Diagnosis is challenging as the phenotypic expression has wide heterogeneity due to variable penetrance of the underlying genetic mutation. Although the condition is inherited in an autosomal dominant pattern, sporadic cases do occur. This report presents a case of a 22-year-old female diagnosed with HDR syndrome, featuring bilateral cataract and bicornuate uterus. The GATA3 mutation detected in the patient was not identified in the family, suggesting it to be arising de novo. The present case report describes the rare phenotypic findings of bilateral cataract and bicornuate uterus associated with HDR, thus expanding the clinical spectrum of the syndrome.},
author = {Chetiwal, Rajesh and Kumar, Amit and Tanwar, Shweta and Rastogi, Priyank},
doi = {10.37349/eemd.2024.00009},
journal = {Exploration of Endocrine and Metabolic Diseases},
pages = {77--82},
title = {{Hypoparathyroidism, deafness and renal dysplasia syndrome with bilateral cataract and bicornuate uterus caused by a de novo GATA3 mutation}},
url = {https://www.explorationpub.com/Journals/eemd/Article/10149},
volume = {1},
year = {2024},
number = {2}
}