AI Article Synopsis

  • Nail-Patella Syndrome (NPS) is a rare genetic disorder characterized by nail and skeletal abnormalities, including issues with patellae, iliac horns, and potential complications like kidney disease and glaucoma.
  • The condition is linked to mutations in the LMX1B gene, which is essential for the development of limbs, kidneys, and eyes.
  • A study of 55 patients and their relatives revealed 38 different LMX1B mutations, with 19 being new discoveries, while 9% of the families studied did not have detectable LMX1B mutations, suggesting possible genetic diversity in NPS.

Article Abstract

Nail-Patella Syndrome (NPS) is a rare autosomal dominant condition comprising nail and skeletal anomalies. Skeletal features include dysplastic patellae and iliac horns, as well as scapula and elbow dysplasia. Nephropathy and glaucoma or intra-ocular hypertension can sometimes be present. NPS is due to variants affecting function in LMX1B, which encodes a LIM-homeodomain protein critical for limb, kidney and eye development. We describe the phenotype and the molecular data of 55 index patients and their 39 relatives presenting with typical NPS. We identified 38 different LMX1B anomalies, 19 of which were not reported before. In our series, 9% of families are not carriers of a LMX1B genomic alteration after extensive study of the coding and non-coding regions of the gene. One of the families showed no linkage to the LMX1B locus, raising the hypothesis of a genetic heterogeneity.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795216PMC
http://dx.doi.org/10.1038/ejhg.2015.77DOI Listing

Publication Analysis

Top Keywords

nail-patella syndrome
8
molecular data
8
raising hypothesis
8
hypothesis genetic
8
genetic heterogeneity
8
syndrome clinical
4
clinical molecular
4
data families
4
families raising
4
heterogeneity nail-patella
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!