Abstract |
The autosomal recessive form of type II cutis laxa (ARCL II) is characterized by the appearance of redundant, inelastic skin with wrinkling, an aged look and additional variable systemic involvement including intrauterine growth retardation, failure to thrive, developmental delay, dysmorphism, osseous abnormality, and CNS manifestations. Several genetic defects have been found in patients and families with the clinical manifestations of ARCL II. Recently, mutations in PYCR1 have been linked to cutis laxa with progeroid features. We ascertained two siblings with of ARCL II born to non-consanguineous parents. Mutation analysis of PYCR1 revealed a novel single-base deletion (c.345delC) in exon 4 leading to frame-shift and premature stop of translation. The effect of this mutation results in a strong reduction of PYCR1 expression in skin fibroblasts from affected siblings. These two cases extend the genotypic spectrum of PYCR1-related ARCL II.
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Authors | Dar-Shong Lin, Chun-Yan Yeung, Hsuan-Liang Liu, Che-Sheng Ho, Chyong-Hsin Shu, Chih-Kuang Chuang, Yu-Wen Huang, Tsu-Yen Wu, Zon-Darr Huang, Yuan-Ren Jian, Shuan-Pei Lin |
Journal | American journal of medical genetics. Part A
(Am J Med Genet A)
Vol. 155A
Issue 6
Pg. 1285-9
(Jun 2011)
ISSN: 1552-4833 [Electronic] United States |
PMID | 21567914
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 Wiley-Liss, Inc. |
Chemical References |
- Pyrroline Carboxylate Reductases
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Topics |
- Aging, Premature
(genetics)
- Base Sequence
- Child
- Cutis Laxa
(genetics, pathology)
- Fibroblasts
(metabolism)
- Frameshift Mutation
(genetics)
- Genes, Recessive
- Genetic Predisposition to Disease
(genetics)
- Humans
- Immunoblotting
- Male
- Molecular Sequence Data
- Pyrroline Carboxylate Reductases
(genetics, metabolism)
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Analysis, DNA
- Skin
(pathology)
- delta-1-Pyrroline-5-Carboxylate Reductase
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