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Journal of Investigative Medicine:
doi: 10.231/JIM.0b013e318250b74c
Original Articles

Identification of Two Novel Mutations in TRPS1 Gene in Families With Tricho-Rhino-Phalangeal Type I Syndrome

Flores-Cuevas, Arturo MD*; Mutchinick, Oswaldo MD; Morales-Suárez, Jose J. MD; González-Huerta, Luz Maria MD; Cuevas-Covarrubias, Sergio A. PhD

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Background: Autosomal dominant tricho-rhino-phalangeal syndrome I (TRPS I) is due to mutations in the TRPS1 gene. Tricho-rhino-phalangeal syndrome I is characterized by peculiar face and skeletal anomalies. Cone-shaped epiphyses are the characteristic radiographic findings.

Objective: To describe 2 families with TRPS I and 2 novel mutations in the TRPS1 gene.

Patients: The study included 2 nonrelated families with TRPS I. All exons of the TRPS1 gene were analyzed from genomic DNA.

Results: The TRPS1 gene mutation analysis showed in family 1 the c.978C>A nonsense mutation within exon 4 and in family 2 the c.164A>C missense mutation within exon 3.

Conclusions: We found 2 families with TRPS1 caused by 2 novel mutations in the TRPS gene, particularly a missense mutation in exon 3, outside the GATA zinc finger domain, that leads a mild TRPS phenotype. Our data show a higher genotypic spectrum in the TRPS I and demonstrate that mutations in the amino terminus of the transcription factor result in TRPS I syndrome.

Copyright © 2012 by the American Federation for Medical Research.


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