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Genetic study identifies a new form of congenital muscular dystrophy

A new form of congenital muscular dystrophy has been discovered which is caused by mutations in a previously un-linked gene.

Genetic study identifies a new form of congenital muscular dystrophy

New gene for CMD

Congenital muscular dystrophy (CMD) is a term used for a group of genetic muscle-wasting conditions, in which the symptoms become apparent at an early age. They cause muscles to weaken and waste over time, leading to increasing disability. They can also cause learning difficulties.

The study, led by our group and Dr Chiara Manzini from George Washington University, examined the DNA of five individuals who were affected by early onset of a group of conditions including muscle weakness and an inability to stand or walk. Although some of the symptoms varied between individuals, the results identified mutations in the same disease gene. Mutations in this gene - INPP5K - had not previously been reported. To get a better idea of the gene’s role in development we blocked the expression of the gene in zebrafish and found that the fish showed muscle damage and eye defects, similar to the features seen in the individuals with the mutations.

The study has been published in the American Journal of Human Genetics. The discovery will allow a precise genetic diagnosis for a greater number of children affected by this condition, and help inform better clinical management. There is currently no treatment available to address the underlying genetic cause of CMD. We hope that further research may identify why a faulty INPP5K gene causes these symptoms – and that information will help with the search for therapies in the future.

 

 

Robert Meadowcroft, Chief Executive of Muscular Dystrophy UK, commented: “Early stage research identifying genes for muscle-wasting conditions, such as this, gives us valuable insight into better understanding these complex and rare conditions. We know families find it extremely difficult living in limbo without a precise diagnosis, particularly in this current era of increasing precision medicine. The results from this paper could help some families living with congenital muscular dystrophy to receive a faster diagnosis, paving the way for a potential treatment for this mutation in the future.”


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