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Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes.

Authors :
Strong A
Skraban C
Meyers K
Amaral S
Furth S
Drant S
Hsiao W
Galea L
Gold J
Gold NB
Leonard J
Lopez S
Zackai EH
Pyeritz RE
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3762-3769. Date of Electronic Publication: 2021 Aug 06.
Publication Year :
2021

Abstract

Heritable connective tissue disorders are a group of diseases, each rare, characterized by various combinations of skin, joint, musculoskeletal, organ, and vascular involvement. Although kidney abnormalities have been reported in some connective tissue disorders, they are rarely a presenting feature. Here we present three patients with prominent kidney phenotypes who were found by whole exome sequencing to have variants in established connective tissue genes associated with Loeys-Dietz syndrome and congenital contractural arachnodactyly. These cases highlight the importance of considering connective tissue disease in children presenting with structural kidney disease and also serves to expand the phenotype of Loeys-Dietz syndrome and possibly congenital contractural arachnodactyly to include cystic kidney disease and cystic kidney dysplasia, respectively.<br /> (© 2021 Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1552-4833
Volume :
185
Issue :
12
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Academic Journal
Accession number :
34355836
Full Text :
https://doi.org/10.1002/ajmg.a.62449