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Genetic study identifies a new form of congenital muscular dystrophy

Date:
February 9, 2017
Source:
University of St George's London
Summary:
A new form of congenital muscular dystrophy has been discovered which is caused by mutations in a previously un-linked gene.
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A new form of congenital muscular dystrophy has been discovered which is caused by mutations in a previously un-linked gene.

The study is 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.

The study, led by Dr Yalda Jamshidi from St George's, University of London 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.

Other symptoms included cataracts, intellectual disability and short stature.

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 the researchers blocked the expression of the gene in zebrafish. They found that the fish then showed muscle damage and eye defects, similar to the features seen in the individuals with the mutations.

Dr Jamshidi said: "These findings can be used for diagnostic testing of people with symptoms similar to those described in this study and where the gene responsible for their condition is not known. If INPP5K is found to be the faulty gene, patients will get better guidance and more accurate information on their condition."

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.

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."

Dr Jamshidi added: "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."


Story Source:

Materials provided by University of St George's London. Note: Content may be edited for style and length.


Journal Reference:

  1. M. Chiara Manzini et al. Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy. American Journal of Human Genetics, February 2017 DOI: 10.1016/j.ajhg.2017.01.019

Cite This Page:

University of St George's London. "Genetic study identifies a new form of congenital muscular dystrophy." ScienceDaily. ScienceDaily, 9 February 2017. <www.sciencedaily.com/releases/2017/02/170209134107.htm>.
University of St George's London. (2017, February 9). Genetic study identifies a new form of congenital muscular dystrophy. ScienceDaily. Retrieved May 29, 2017 from www.sciencedaily.com/releases/2017/02/170209134107.htm
University of St George's London. "Genetic study identifies a new form of congenital muscular dystrophy." ScienceDaily. www.sciencedaily.com/releases/2017/02/170209134107.htm (accessed May 29, 2017).

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