RMRP gene sequence analysis confirms a cartilage-hair hypoplasia variant with only skeletal manifestations and reveals a high density of single-nucleotide polymorphisms
Article first published online: 3 APR 2002
Volume 61, Issue 2, pages 146–151, February 2002
How to Cite
Bonafé, L., Schmitt, K., Eich, G., Giedion, A. and Superti-Furga, A. (2002), RMRP gene sequence analysis confirms a cartilage-hair hypoplasia variant with only skeletal manifestations and reveals a high density of single-nucleotide polymorphisms. Clinical Genetics, 61: 146–151. doi: 10.1034/j.1399-0004.2002.610210.x
- Issue published online: 3 APR 2002
- Article first published online: 3 APR 2002
- Received 29 October 2001, revised and accepted for publication 3 December 2001
- cartilage-hair hypoplasia;
- genetic mutations;
- metaphyseal dysplasia;
- RMRP gene;
- single-nucleotide polymorphisms
Mutations in the RMRP gene that codes for an RNA subunit of the MRP RNAse complex are the cause of cartilage-hair hypoplasia (CHH; MIM 250250). We tested the hypothesis that recessive metaphyseal dysplasia without hypotrichosis (M1M 250460), a disorder presenting with short stature and metaphyseal dysplasia similar to CHH, but lacking hair anomalies, immunodeficiency and other extra skeletal features, might be allelic to CHH. We identified four mutation-carrying alleles segregating with the skeletal phenotype in two unrelated boys and their parents. One allele carried the common Finnish mutation +70A → G; the remaining three carried +195C → T, +238C → T, and dupAAGCTGAGGACG at −2. Sequencing 120 alleles from a control group revealed an unusually high density of single-nucleotide polymorphisms in and around the RMRP gene: the biological significance of this finding is unclear.
We conclude that recessive metaphyseal dysplasia without hypotrichosis is a variant of CHH, manifesting only as short stature and metaphyseal dysplasia. Precise diagnosis of this form of metaphyseal dysplasia is not without importance because of recessive inheritance with corresponding recurrence risk, as well as because of potential complications such as anaemia, susceptibility to infections and the increased likelihood of developing cancer. The short stature and metaphyseal changes associated with cone-shaped epiphyses of the hands should raise the diagnostic possibility of a CHH-related disorder that can then be confirmed by mutation analysis.