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Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes.
- 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.)
- Subjects :
- Adolescent
Arachnodactyly complications
Arachnodactyly diagnostic imaging
Arachnodactyly pathology
Child
Connective Tissue pathology
Connective Tissue Diseases complications
Connective Tissue Diseases diagnostic imaging
Connective Tissue Diseases genetics
Connective Tissue Diseases pathology
Contracture complications
Contracture diagnostic imaging
Contracture pathology
Genetic Predisposition to Disease
Humans
Kidney diagnostic imaging
Kidney pathology
Kidney Diseases, Cystic complications
Kidney Diseases, Cystic genetics
Kidney Diseases, Cystic pathology
Loeys-Dietz Syndrome complications
Loeys-Dietz Syndrome diagnostic imaging
Loeys-Dietz Syndrome pathology
Male
Mutation genetics
Phenotype
Skin Abnormalities complications
Skin Abnormalities genetics
Skin Abnormalities pathology
Exome Sequencing
Arachnodactyly genetics
Contracture genetics
Fibrillin-2 genetics
Loeys-Dietz Syndrome genetics
Receptor, Transforming Growth Factor-beta Type I genetics
Smad2 Protein genetics
Subjects
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