Literature DB >> 28717939

Neonatal stroke and haematuria: Answers.

Sally Kellett1,2, Mathieu Lemaire3,4, Steven P Miller4,5, Christoph Licht3,4, Grace Yoon4,6, Nomazulu Dlamini4,5, Damien Noone3,4.   

Abstract

BACKGROUND: This is a report of an infant born near term with neonatal stroke and haematuria. The renal phenotype, pathogenic genotype and pathological findings on renal biopsy are discussed. CASE-DIAGNOSIS: Prenatal magnetic resonance imaging revealed anomalies which persisted postnatally. Haematuria was detected during follow-up. The posttnatal renal ultrasound scan was normal, and there was no associated proteinuria. A likely pathogenic genetic mutation was detected.
CONCLUSIONS: This case highlights a relatively newly discovered cause of hereditary nephropathy in which the basement membrane is affected, with initial effects on the glomerular membranes and subsequent effects on the renal tubular basement membranes.

Entities:  

Keywords:  COL4A1 mutations; Glomerulocystic disease; HANAC; Hereditary nephropathy; Renal biopsy

Mesh:

Substances:

Year:  2017        PMID: 28717939     DOI: 10.1007/s00467-017-3747-8

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  22 in total

1.  Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis.

Authors:  R Kalluri; C F Shield; P Todd; B G Hudson; E G Neilson
Journal:  J Clin Invest       Date:  1997-05-15       Impact factor: 14.808

Review 2.  CNS vasculitis and stroke in neonatal lupus erythematosus: a case report and review of literature.

Authors:  Arushi G Saini; Naveen Sankhyan; Sagar Bhattad; Sameer Vyas; Biman Saikia; Pratibha Singhi
Journal:  Eur J Paediatr Neurol       Date:  2014-01-25       Impact factor: 3.140

Review 3.  Mammalian collagen receptors.

Authors:  Birgit Leitinger; Erhard Hohenester
Journal:  Matrix Biol       Date:  2006-11-10       Impact factor: 11.583

4.  Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.

Authors:  Douglas B Gould; F Campbell Phalan; Guido J Breedveld; Saskia E van Mil; Richard S Smith; John C Schimenti; Umberto Aguglia; Marjo S van der Knaap; Peter Heutink; Simon W M John
Journal:  Science       Date:  2005-05-20       Impact factor: 47.728

Review 5.  Clinical spectrum of type IV collagen (COL4A1) mutations: a novel genetic multisystem disease.

Authors:  Katayoun Vahedi; Sonia Alamowitch
Journal:  Curr Opin Neurol       Date:  2011-02       Impact factor: 5.710

6.  A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.

Authors:  Ganeshwaran H Mochida; Vijay S Ganesh; Jillian M Felie; Danielle Gleason; R Sean Hill; Katie Rose Clapham; Daniel Rakiec; Wen-Hann Tan; Nadia Akawi; Muna Al-Saffar; Jennifer N Partlow; Sigrid Tinschert; A James Barkovich; Bassam Ali; Lihadh Al-Gazali; Christopher A Walsh
Journal:  Am J Hum Genet       Date:  2010-11-25       Impact factor: 11.025

Review 7.  Alport syndrome and thin basement membrane nephropathy.

Authors:  Paul Scott Thorner
Journal:  Nephron Clin Pract       Date:  2007-06-06

8.  COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage.

Authors:  Linda S de Vries; Corine Koopman; Floris Groenendaal; Mary Van Schooneveld; Frans W Verheijen; Elly Verbeek; Theo D Witkamp; H Bart van der Worp; Grazia Mancini
Journal:  Ann Neurol       Date:  2009-01       Impact factor: 10.422

Review 9.  The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature.

Authors:  Marije E C Meuwissen; Dicky J J Halley; Liesbeth S Smit; Maarten H Lequin; Jan M Cobben; René de Coo; Jeske van Harssel; Suzanne Sallevelt; Gwendolyn Woldringh; Marjo S van der Knaap; Linda S de Vries; Grazia M S Mancini
Journal:  Genet Med       Date:  2015-02-26       Impact factor: 8.822

10.  COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle cramps.

Authors:  Emmanuelle Plaisier; Olivier Gribouval; Sonia Alamowitch; Béatrice Mougenot; Catherine Prost; Marie Christine Verpont; Béatrice Marro; Thomas Desmettre; Salomon Yves Cohen; Etienne Roullet; Michel Dracon; Michel Fardeau; Tom Van Agtmael; Dontscho Kerjaschki; Corinne Antignac; Pierre Ronco
Journal:  N Engl J Med       Date:  2007-12-27       Impact factor: 91.245

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