Literature DB >> 25638216

Renal involvement in children with HNF1β mutation: early sonographic appearances and long-term follow-up.

Fred E Avni1, Annie Lahoche, Carole Langlois, Catherine Garel, Michele Hall, Pierre-Hugues Vivier.   

Abstract

OBJECTIVES: The aim was to report ultrasound (US) patterns of hepatocyte nuclear factor (HNF1β) mutation throughout childhood and determine whether ultrasound could be predictive of renal failure.
METHODS: The sonographic examinations in 34 children with HNF1β mutation were reviewed. Their sonographic characteristics were compared with renal function.
RESULTS: At first postnatal examination renal length was normal in 44 % of the patients, decreased in 24 %, increased in 12 % and asymmetrical in 20 %. Renal cortex was hyperechoic in 97 %. Corticomedullary differentiation was abnormal in 59 %. Cysts were present in 77 % of patients. Cysts were mostly subcapsular (64 %). Twenty-eight patients had follow-up examinations. A modification of the sonographic appearance was observed in 91 % of patients. Eight patients (23 %) had renal failure; no specific US pattern could be demonstrated.
CONCLUSIONS: At birth, HNF1β mutation was typically associated on US with the combination of hyperechoic, normal-sized kidneys with abnormal corticomedullary differentiation (CMD) and multiple cortical cysts. In older children, the appearances can be variable: kidneys may have decreased (32 %) or normal size (33 %); they are usually hyperechoic (50 %) with abnormal CMD (78 %) and (sub)cortical cysts (71 %). No pattern appears to be associated with renal failure. KEY POINTS: • HNF1β mutations determine significant anomalies of sonographic appearances of kidneys in children. • Kidneys appear mainly hyperechoic, with or without CMD and with subcapsular cysts. • The US pattern may evolve throughout childhood in the same patient. • No correlation was found between any sonographic pattern and renal failure.

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Year:  2015        PMID: 25638216     DOI: 10.1007/s00330-014-3550-x

Source DB:  PubMed          Journal:  Eur Radiol        ISSN: 0938-7994            Impact factor:   5.315


  15 in total

1.  Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort.

Authors:  Tim Ulinski; Sandra Lescure; Sandrine Beaufils; Vincent Guigonis; Stéphane Decramer; Denis Morin; Séverine Clauin; Georges Deschênes; François Bouissou; Albert Bensman; Christine Bellanné-Chantelot
Journal:  J Am Soc Nephrol       Date:  2005-12-21       Impact factor: 10.121

2.  Fetal kidneys: additional sonographic criteria of normal development.

Authors:  Arnaud Devriendt; Marie Cassart; Anne Massez; Catherine Donner; Fred E Avni
Journal:  Prenat Diagn       Date:  2013-10-07       Impact factor: 3.050

3.  Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations.

Authors:  Coralie Bingham; Sian Ellard; Trevor R P Cole; Katrin E Jones; Lisa I S Allen; Judith A Goodship; Timothy H J Goodship; Daniela Bakalinova-Pugh; Gavin I Russell; Adrian S Woolf; Anthony J Nicholls; Andrew T Hattersley
Journal:  Kidney Int       Date:  2002-04       Impact factor: 10.612

4.  Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys.

Authors:  Stéphane Decramer; Olivier Parant; Sandrine Beaufils; Séverine Clauin; Cécile Guillou; Sylvie Kessler; Jacqueline Aziza; Flavio Bandin; Joost P Schanstra; Christine Bellanné-Chantelot
Journal:  J Am Soc Nephrol       Date:  2007-01-31       Impact factor: 10.121

5.  HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.

Authors:  Makiko Nakayama; Kandai Nozu; Yuki Goto; Koichi Kamei; Shuichi Ito; Hidenori Sato; Mitsuru Emi; Koichi Nakanishi; Shigeru Tsuchiya; Kazumoto Iijima
Journal:  Pediatr Nephrol       Date:  2010-02-13       Impact factor: 3.714

Review 6.  Imaging and classification of congenital cystic renal diseases.

Authors:  Fred E Avni; Catherine Garel; Marie Cassart; Nicky D'Haene; Michele Hall; Michael Riccabona
Journal:  AJR Am J Roentgenol       Date:  2012-05       Impact factor: 3.959

7.  HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.

Authors:  Shazia Adalat; Adrian S Woolf; Karen A Johnstone; Andrea Wirsing; Lorna W Harries; David A Long; Raoul C Hennekam; Sarah E Ledermann; Lesley Rees; William van't Hoff; Stephen D Marks; Richard S Trompeter; Kjell Tullus; Paul J Winyard; Janette Cansick; Imran Mushtaq; Harjeeta K Dhillon; Coralie Bingham; Emma L Edghill; Rukshana Shroff; Horia Stanescu; Gerhart U Ryffel; Sian Ellard; Detlef Bockenhauer
Journal:  J Am Soc Nephrol       Date:  2009-04-23       Impact factor: 10.121

8.  Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations.

Authors:  Christine Bellanné-Chantelot; Dominique Chauveau; Jean-François Gautier; Danièle Dubois-Laforgue; Séverine Clauin; Sandrine Beaufils; Jean-Marie Wilhelm; Christian Boitard; Laure-Hélène Noël; Gilberto Velho; José Timsit
Journal:  Ann Intern Med       Date:  2004-04-06       Impact factor: 25.391

Review 9.  [Abnormalities of hepatocyte nuclear factor (HNF)-1beta: biological mechanisms, phenotypes, and clinical consequences].

Authors:  T Ulinski; A Bensman; S Lescure
Journal:  Arch Pediatr       Date:  2009-04-09       Impact factor: 1.180

10.  Different phenotypes of HNF1ß deletion mutants in familial multicystic dysplastic kidneys.

Authors:  Masafumi Hasui; Kazunari Kaneko; Shoji Tsuji; Yuka Isozaki; Takahisa Kimata; Yoshimi Nozu; Kandai Nozu; Kazumoto Iijima
Journal:  Clin Nephrol       Date:  2013-06       Impact factor: 0.975

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  2 in total

1.  The "salt and pepper" pattern on renal ultrasound in a group of children with molecular-proven diagnosis of ciliopathy-related renal diseases.

Authors:  Pauline Iorio; Laurence Heidet; Caroline Rutten; Nicolas Garcelon; Marie-Pierre Audrézet; Vincent Morinière; Nathalie Boddaert; Rémi Salomon; Laureline Berteloot
Journal:  Pediatr Nephrol       Date:  2020-02-10       Impact factor: 3.714

2.  Spectrum of Mutations in Pediatric Non-glomerular Chronic Kidney Disease Stages 2-5.

Authors:  Xiaoyuan Wang; Huijie Xiao; Yong Yao; Ke Xu; Xiaoyu Liu; Baige Su; Hongwen Zhang; Na Guan; Xuhui Zhong; Yanqin Zhang; Jie Ding; Fang Wang
Journal:  Front Genet       Date:  2021-07-06       Impact factor: 4.599

  2 in total

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