A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation
Abstract Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3, but presenting no renal dysplasia or family histor...
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Bibliographic Details
| Main Authors: |
Haruka Kishi,
Teruo Jojima,
Takahiko Kogai,
Toshie Iijima,
Eriko Ohira,
Dai Tanuma,
Sachiyo Konno,
Kanako Kato,
Atsumi Kezuka,
Kazumi Akimoto,
Junko Sakumoto,
Akira Hishinuma,
Takuya Tomaru,
Noriko Makita,
Isao Usui,
Yoshimasa Aso |
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| Format: | Article
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| Language: | English |
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| Published: |
Wiley
2020-12-01
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| Series: | Clinical Case Reports
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| Subjects: |
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| Online Access: | https://doi.org/10.1002/ccr3.3186
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