Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity.

ABSTRACT:

Background

Elastin gene mutations have been associated with a variety of phenotypes. Autosomal dominant cutis laxa (ADCL) is a rare disorder that presents with lax skin, typical facial characteristics, inguinal hernias, aortic root dilatation and pulmonary emphysema. In most patients, frameshift mutations are found in the 3' region of the elastin gene (exons 30-34) which result in a C-terminally extended protein, though exceptions have been reported.

Methods

We clinically and molecularly characterized the thus far largest cohort of ADCL patients, consisting of 19 patients from six families and one sporadic patient.

Results

Molecular analysis showed C-terminal frameshift mutations in exon 30, 32, and 34 of the elastin gene and identified a mutational hotspot in exon 32

SUBMITTER: Hadj-Rabia S 

PROVIDER: S-EPMC3599008 | biostudies-literature | 2013 Feb

REPOSITORIES: biostudies-literature