Literature DB >> 28621010

Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports.

Takahisa Yoshikawa1, Koichi Kamei1, Hiroko Nagata1, Ken Saida1, Mai Sato1, Masao Ogura1, Shuichi Ito1,2, Osamu Miyazaki3, Maki Urushihara4, Shuji Kondo4, Noriko Sugawara5, Kiyonobu Ishizuka5, Yuko Hamasaki6, Seiichiro Shishido6, Naoya Morisada7,8, Kazumoto Iijima7, Michio Nagata9, Takako Yoshioka10, Kentaro Ogata11, Kenji Ishikura1.   

Abstract

WDR19 has been reported as a causative gene of nephronophthisis-related ciliopathies. Patients with WDR19 mutations can show various extrarenal manifestations such as skeletal disorders, Caroli disease, and retinal dystrophy, and typically display nephronophthisis as a renal phenotype. However, there is limited information on the renal phenotypes of patients with WDR19 mutations. We report two Japanese infants with Sensenbrenner syndrome caused by WDR19 mutations who demonstrated different features in renal ultrasound and histopathological results, despite several common extrarenal manifestations. Patient 1 had normal sized and hyperechogenic kidneys with several small cysts and histopathological findings compatible with infantile nephronophthisis. Renal ultrasound of Patient 2 showed enlarged kidneys with diffuse microcysts resembling those of autosomal recessive polycystic kidney disease. Her renal histopathology revealed dysplastic kidney with diffuse glomerular cysts. Genetic testing identified compound heterozygous mutations in WDR19 in both patients (Patient 1: c.953delA, c.3533G > A, Patient 2: c.2645 + 1G > T, c.3533G > A). Our patients suggest that WDR19 mutations can cause dysplastic kidney in addition to nephronophthisis pathologically. In addition, differences in pathology of the kidneys from WDR19 mutations may result in heterogeneous features in renal ultrasound findings. Renal phenotypes from WDR19 mutations may thus be more diverse than previously reported. Extrarenal manifestations and genetic testing can therefore help to diagnosis this disease more precisely.
© 2017 Asian Pacific Society of Nephrology.

Entities:  

Keywords:  WDR19; ciliopathy; dysplastic kidney; glomerular cyst; nephronophthisis

Mesh:

Substances:

Year:  2017        PMID: 28621010     DOI: 10.1111/nep.12996

Source DB:  PubMed          Journal:  Nephrology (Carlton)        ISSN: 1320-5358            Impact factor:   2.506


  2 in total

1.  Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome.

Authors:  Ai Unzaki; Naoya Morisada; Kandai Nozu; Ming Juan Ye; Shuichi Ito; Tatsuo Matsunaga; Kenji Ishikura; Shihomi Ina; Koji Nagatani; Takayuki Okamoto; Yuji Inaba; Naoko Ito; Toru Igarashi; Shoichiro Kanda; Ken Ito; Kohei Omune; Takuma Iwaki; Kazuyuki Ueno; Mayumi Yahata; Yasufumi Ohtsuka; Eriko Nishi; Nobuya Takahashi; Tomoaki Ishikawa; Shunsuke Goto; Nobuhiko Okamoto; Kazumoto Iijima
Journal:  J Hum Genet       Date:  2018-03-02       Impact factor: 3.172

2.  Case Report: Sequential Liver After Kidney Transplantation in a Patient With Sensenbrenner Syndrome (Cranioectodermal Dysplasia).

Authors:  Joanna Ryżko; Joanna Walczak-Sztulpa; Piotr Czubkowski; Anna Latos-Bieleńska; Adam Kowalski; Marek Stefanowicz; Wioletta Jarmużek; Ryszard Grenda; Joanna Pawłowska
Journal:  Front Pediatr       Date:  2022-02-25       Impact factor: 3.418

  2 in total

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