Literature DB >> 9894834

Diffuse mesangial sclerosis: association with unreported congenital anomalies and placental enlargement.

E Mildenberger1, T Lennert, J Kunze, C Jandeck, R Waldherr, H Versmold.   

Abstract

A case of diffuse mesangial sclerosis (DMS) associated with a number of undescribed congenital anomalies is reported. The occurrence of additional anomalies, especially ocular anomalies, is a common finding in DMS. However, neither megalocornea, Dandy-Walker malformation, postaxial hexadactyly, rocker-bottom feet, nor atrial septal defect, as observed in our patient, has been reported previously in association with DMS. This case might be considered an atypical manifestation of the Galloway-Mowat syndrome. In contrast to most cases of DMS, the patient revealed intrauterine proteinuria as the placenta was enlarged to 31% of birth weight. This case demonstrates that the large placenta, >25% of birth weight, is not only pathognomonic of the congenital nephrotic syndrome of the Finnish type but can also occur in DMS.

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Year:  1998        PMID: 9894834     DOI: 10.1080/080352598750031022

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  5 in total

1.  Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome.

Authors:  Andreas Dietrich; Verena Matejas; Martin Bitzan; Seema Hashmi; Cathy Kiraly-Borri; Shuan-Pei Lin; Eva Mildenberger; Bernd Hoppe; Lars Palm; Takashi Shiihara; Jens-Oliver Steiss; Jeng-Daw Tsai; Udo Vester; Stefanie Weber; Elke Wühl; Kristina Zepf; Martin Zenker
Journal:  Pediatr Nephrol       Date:  2008-07-02       Impact factor: 3.714

2.  A case of atypical congenital nephrotic syndrome.

Authors:  Janusz Swietliński; Iwona Maruniak-Chudek; Zofia I Niemir; Aldona Woźniak; Maria Wilińska; Joanna Zacharzewska
Journal:  Pediatr Nephrol       Date:  2004-01-09       Impact factor: 3.714

3.  Eye involvement in children with primary focal segmental glomerulosclerosis.

Authors:  Fatih Ozaltin; Saskia Heeringa; Ceren Erdogan Poyraz; Yelda Bilginer; Sibel Kadayifcilar; Nesrin Besbas; Rezan Topaloglu; Seza Ozen; Friedhelm Hildebrandt; Aysin Bakkaloglu
Journal:  Pediatr Nephrol       Date:  2007-12-05       Impact factor: 3.714

Review 4.  Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum.

Authors:  Verena Matejas; Bernward Hinkes; Faisal Alkandari; Lihadh Al-Gazali; Ellen Annexstad; Mehmet B Aytac; Margaret Barrow; Kveta Bláhová; Detlef Bockenhauer; Hae Il Cheong; Iwona Maruniak-Chudek; Pierre Cochat; Jörg Dötsch; Priya Gajjar; Raoul C Hennekam; Françoise Janssen; Mikhail Kagan; Ariana Kariminejad; Markus J Kemper; Jens Koenig; Jillene Kogan; Hester Y Kroes; Eberhard Kuwertz-Bröking; Amy F Lewanda; Ana Medeira; Jutta Muscheites; Patrick Niaudet; Michel Pierson; Anand Saggar; Laurie Seaver; Mohnish Suri; Alexey Tsygin; Elke Wühl; Aleksandra Zurowska; Steffen Uebe; Friedhelm Hildebrandt; Corinne Antignac; Martin Zenker
Journal:  Hum Mutat       Date:  2010-09       Impact factor: 4.878

5.  Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome.

Authors:  Nina Mann; Slim Mzoughi; Ronen Schneider; Susanne J Kühl; Denny Schanze; Verena Klämbt; Svjetlana Lovric; Youying Mao; Shasha Shi; Weizhen Tan; Michael Kühl; Ana C Onuchic-Whitford; Ernestine Treimer; Thomas M Kitzler; Franziska Kause; Sven Schumann; Makiko Nakayama; Florian Buerger; Shirlee Shril; Amelie T van der Ven; Amar J Majmundar; Kristina Marie Holton; Amy Kolb; Daniela A Braun; Jia Rao; Tilman Jobst-Schwan; Eva Mildenberger; Thomas Lennert; Alma Kuechler; Dagmar Wieczorek; Oliver Gross; Beate Ermisch-Omran; Anja Werberger; Martin Skalej; Andreas R Janecke; Neveen A Soliman; Shrikant M Mane; Richard P Lifton; Jan Kadlec; Ernesto Guccione; Michael J Schmeisser; Martin Zenker; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2021-02-16       Impact factor: 10.121

  5 in total

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