Analysis of genes encoding laminin β2 and related proteins in patients with Galloway

Analysis of genes encoding laminin β2 and related proteins in patients with Galloway–Mowat syndrome

Published:2008-10 Issue:10 Volume:23 Page:1779-1786
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Dietrich Andreas,Matejas Verena,Bitzan Martin,Hashmi Seema,Kiraly-Borri Cathy,Lin Shuan-Pei,Mildenberger Eva,Hoppe Bernd,Palm Lars,Shiihara Takashi,Steiss Jens-Oliver,Tsai Jeng-Daw,Vester Udo,Weber Stefanie,Wühl Elke,Zepf Kristina,Zenker Martin

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-008-0880-4.pdf

Reference35 articles.

1. Cooperstone BG, Friedman A, Kaplan BS (1993) Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy. Am J Med Genet 47:250–254

2. Galloway WH, Mowat AP (1968) Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs. J Med Genet 5:319–321

3. de Vries BB, van’tHoff WG, Surtees RA, Winter RM (2001) Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay. Clin Dysmorphol 10:115–121

4. Meyers KE, Kaplan P, Kaplan BS (1999) Nephrotic syndrome, microcephaly, and developmental delay: three separate syndromes. Am J Med Genet 82:257–260

5. Cohen AH, Turner MC (1994) Kidney in Galloway-Mowat syndrome: clinical spectrum with description of pathology. Kidney Int 45:1407–1415

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