Unusual Proliferative Glomerulonephritis in a Patient Diagnosed to Have Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome with a Novel Mutation in the GATA3 Gene.
Intern Med
; 56(11): 1393-1397, 2017.
Article
em En
| MEDLINE
| ID: mdl-28566604
ABSTRACT
Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is a rare autosomal dominant disease caused by GATA3 mutations. Although several cases with variable renal features have been reported, the presence of histological changes within the glomeruli in adult patients is unclear. We herein report an adult case of HDR syndrome with a novel p.C288W (TGC>TGG) missense mutation in GATA3. His renal histology showed a membranoproliferative glomerulonephritis-like glomerular lesion. Additional renal histological analyses of HDR syndrome patients will be needed to clarify the role of GATA3 in both the developing and adult kidney.
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Base de dados:
MEDLINE
Assunto principal:
Glomerulonefrite
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Perda Auditiva Neurossensorial
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Hipoparatireoidismo
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Nefrose
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article