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A novel mutation in CDMP1 causes brachydactyly type C with "angel-shaped phalanx". A genotype-phenotype correlation in the mutational spectrum.
- Source :
-
European journal of medical genetics [Eur J Med Genet] 2012 Nov; Vol. 55 (11), pp. 611-4. Date of Electronic Publication: 2012 Jul 22. - Publication Year :
- 2012
-
Abstract
- Brachydactyly type C (BDC), a well-recognized autosomal dominant hand malformation, displays brachymesophalangy of the second, third, and fifth fingers, a short first metacarpal, hyperphalangy, and ulnar deviation of the index finger. An "angel-shaped phalanx" is a distinctive radiological sign that can be found in BDC and other skeletal dysplasias, such as angel-shaped phalango-epiphyseal dysplasia (ASPED), an autosomal dominant skeletal abnormality characterized by a typical angel-shaped phalanx, brachydactyly, specific radiological findings, abnormal dentition, hip dysplasia, and delayed bone age. BDC and ASPED result from mutations in the CDMP1 gene. We report here a Mexican patient with BDC and clinical features of ASPED who carries a novel mutation in CDMP1, confirming that BDC and ASPED are part of the CDMP1 mutational spectrum. Based on the large number of clinical features in common, we suggest that both anomalies are part of the same clinical spectrum. Supported by an extensive review of the literature, a possible genotype-phenotype correlation in the mutational spectrum of this gene is proposed.<br /> (Copyright © 2012 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Bone Diseases, Developmental diagnosis
Bone Diseases, Developmental diagnostic imaging
Brachydactyly diagnosis
Brachydactyly diagnostic imaging
Child
Epiphyses diagnostic imaging
Fingers abnormalities
Frameshift Mutation
Genetic Association Studies
Heterozygote
Humans
Male
Radiography
Sequence Deletion
Bone Diseases, Developmental genetics
Brachydactyly genetics
Growth Differentiation Factor 5 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1878-0849
- Volume :
- 55
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- European journal of medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 22828468
- Full Text :
- https://doi.org/10.1016/j.ejmg.2012.07.004