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A novel elastin gene mutation in a Vietnamese patient with cutis laxa
Mark L Siefring1, Elizabeth C Lawrence, Tom C Nguyen
1Stamford Skin and Medical Centre, Ho Chi Minh City, Vietnam.
Abstract:
We report a 3-year-old girl from Vietnam with severe congenital cutis laxa; no cardiovascular, pulmonary, neurologic, or visceral involvement; and no family history of cutis laxa. Mutational analysis of the elastin gene identified heterozygosity for a previously unreported de novo c.2184delT mutation in exon 30 not present in either parent.
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