Cargando…

Tumoral calcinosis in a patient with hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome undergoing hemodialysis

We describe a hemodialysis patient with hypoparathyroidism due to HDR (hypoparathyroidism, sensorineural deafness, and renal dysplasia) syndrome caused by GATA3 mutation. She presents tumoral calcinosis which is a rare complication of end-stage renal failure. A novel mutation of GATA3 is identified...

Descripción completa

Detalles Bibliográficos
Autores principales:	Hiramatsu, Rikako, Ubara, Yoshifumi, Tajima, Toshihiro, Usui, Takeshi, Namba, Kazutaka, Takeuchi, Yasuhiro, Sawa, Naoki, Hasegawa, Eiko, Takaichi, Kenmei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BlackWell Publishing Ltd 2015
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352355/ https://www.ncbi.nlm.nih.gov/pubmed/25767699 http://dx.doi.org/10.1002/ccr3.125

Ejemplares similares

Bone Histology of Two Cases with Osteomalacia Related to Low-dose Adefovir
por: Hiramatsu, Rikako, et al.
Publicado: (2016)

Hemodialysis without Anticoagulation for a Patient with Chronic Disseminated Intravascular Coagulation
por: Yamanouchi, Masayuki, et al.
Publicado: (2014)

Lung squamous cell carcinoma associated with hypoparathyroidism with sensorineural deafness and renal dysplasia syndrome: a case report
por: Kojima, Mariko, et al.
Publicado: (2018)

Myeloperoxidase-antineutrophil cytoplasmic antibody-associated crescentic glomerulonephritis in autosomal dominant polycystic kidney disease
por: Sumida, Keiichi, et al.
Publicado: (2013)

Membranoproliferative glomerulonephritis and circulating cryoglobulins
por: Hiramatsu, Rikako, et al.
Publicado: (2013)

Efficacy of Secukinumab for Plaque Psoriasis in a Patient on Hemodialysis
por: Ikuma, Daiuske, et al.
Publicado: (2019)

The First Turkish Case of Hypoparathyroidism, Deafness and Renal Dysplasia (HDR) Syndrome
por: Döneray, Hakan, et al.
Publicado: (2015)

Quality of life of patients with ADPKD—Toranomon PKD QOL study: cross-sectional study
por: Suwabe, Tatsuya, et al.
Publicado: (2013)

Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease
por: Hasegawa, Eiko, et al.
Publicado: (2016)

Intracystic magnetic resonance imaging in patients with autosomal dominant polycystic kidney disease: features of severe cyst infection in a case–control study
por: Suwabe, Tatsuya, et al.
Publicado: (2016)

Renal prognosis a long time after renal biopsy on patients with diabetic nephropathy
por: Mise, Koki, et al.
Publicado: (2014)

Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically
por: Imafuku, Aya, et al.
Publicado: (2018)

Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report
por: Mise, Koki, et al.
Publicado: (2013)

HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Hirschsprung Disease
por: Sepahi, Mohsen Akhavan, et al.
Publicado: (2010)

Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a GATA3 mutation
por: Shim, Yong Suk, et al.
Publicado: (2015)

Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Syndrome Presenting With Febrile Seizures and Hypocalcemia
por: Gandolfi, Anne, et al.
Publicado: (2023)

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
por: Kamezaki, Michitsugu, et al.
Publicado: (2017)

Variegate porphyria complicated by systemic AA amyloidosis: a case report
por: Tsuchiya, Yoshiki, et al.
Publicado: (2013)

Two Types of Renovascular Lesions in Lupus Nephritis with Clinical Thrombotic Thrombocytopenic Purpura
por: Sekine, Akinari, et al.
Publicado: (2015)

Eltrombopag Improves Refractory Thrombocytopenia in a Patient with Systemic Lupus Erythematosus
por: Shima, Natsuki, et al.
Publicado: (2018)

Tolvaptan for Primary Aldosteronism and Autosomal Dominant Polycystic Kidney Disease: A Case Report
por: Kunizawa, Kyohei, et al.
Publicado: (2018)

Characteristic Renal Histology of a 81-Year-Old Patient with a 30-Year History of Diabetes Mellitus: A Case Report
por: Shima, Natsuki, et al.
Publicado: (2020)

Corticosteroid reduction by addition of cetirizine and montelukast in biopsy-proven minimal-change nephrotic syndrome concomitant with allergic disorders
por: Oshima, Yoichi, et al.
Publicado: (2020)

Denosumab for dialysis patients with osteoporosis: A cohort study
por: Kunizawa, Kyohei, et al.
Publicado: (2020)

A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome
por: Chu, Xue-Ying, et al.
Publicado: (2017)

Effect of Proteinuria and Glomerular Filtration Rate on Renal Outcome in Patients with Biopsy-Proven Benign Nephrosclerosis
por: Sumida, Keiichi, et al.
Publicado: (2016)

Tolvaptan for the Treatment of Enlarged Polycystic Liver Disease
por: Mizuno, Hiroki, et al.
Publicado: (2017)

PKD1-associated autosomal dominant polycystic kidney disease with glomerular cysts presenting with nephrotic syndrome caused by focal segmental glomerulosclerosis
por: Oda, Yasuhiro, et al.
Publicado: (2019)

Long-term Low-density Lipoprotein Apheresis in a Patient with Refractory Idiopathic Membranous Glomerulonephritis
por: Yabuuchi, Junko, et al.
Publicado: (2017)

Brain calcinosis in a dialysis patient with hypoparathyroidism
por: Gionanlis, Lazaros, et al.
Publicado: (2008)

The Long-term Outcomes after VAD plus SCT Therapy in a Patient with AL Amyloidosis and Severe Factor X Deficiency
por: Iwadate, Dosuke, et al.
Publicado: (2017)

A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4
por: Sakoh, Takashi, et al.
Publicado: (2019)

Renal-Limited Thrombotic Microangiopathy due to Bevacizumab Therapy for Metastatic Colorectal Cancer: A Case Report
por: Toriu, Naoya, et al.
Publicado: (2019)

Arteriovenous fistula-related renal bleeding 5 days after percutaneous renal biopsy
por: Shima, Natsuki, et al.
Publicado: (2019)

Ahsa1 and Hsp90 activity confers more severe craniofacial phenotypes in a zebrafish model of hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR)
por: Sheehan-Rooney, Kelly, et al.
Publicado: (2013)

Preservation of renal function by intensive glycemic control
por: Toriu, Naoya, et al.
Publicado: (2018)

Brown tumor diagnosed three years after parathyroidectomy in a patient with nail-patella syndrome: A case report
por: Toriu, Naoya, et al.
Publicado: (2018)

Significance of urinary albumin excretion in patients with cast nephropathy
por: Nakagawa, Ryo, et al.
Publicado: (2019)

AA Amyloidosis and Atypical Familial Mediterranean Fever with Exon 2 and 3 Mutations
por: Yabuuchi, Junko, et al.
Publicado: (2017)

Effect of online hemodiafiltration compared with hemodialysis on quality of life in patients with ESRD: A systematic review and meta-analysis of randomized trials
por: Suwabe, Tatsuya, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_t67up0m1gdcjcct2lef15kocko