The discovery of genes like PAX5 improves diagnostic testing for neurodevelopmental disorders, and more

Discovering new genes that are linked to undiagnosed diseases not only has important scientific and clinical consequences, but it also carries important personal implications for patients.

Unraveling the genetic basis of neurological conditions has important implications for basic science, the clinic and the personal lives of patients.

For instance, a study by a team of researchers at Baylor College of Medicine of a novel neurodevelopmental disorder resulted in the discovery of associated mutations or deletions affecting a gene called PAX5.

Led by corresponding author Dr. Daryl Scott, the Baylor team connected with researchers around the globe who studied PAX5 using an online site called GeneMatcher. Working together, the group described 16 patients who exhibited similar characteristics, including developmental delay, intellectual disability and autism spectrum disorder. Some patients also experienced seizures and hearing loss.

Dr. Daryl Scott

The researchers also examined data from the International Mouse Phenotyping Consortium and discovered that defects in Pax5 caused similar symptoms in mouse models.

A better understanding of a neurodevelopmental disorder carries important clinical implications

“The data show that PAX5 is a gene that causes medical problems even if only one copy is mutated or deleted,” said Scott, associate professor in the Department of Molecular and Human Genetics at Baylor.

This gene also stood out as being really important for normal brain function in mouse models, which mirrored what we saw in our patients.”

Patients in the cohort did not have a recurrent pattern of abnormal brain MRI findings, structural birth defects or dysmorphic features. Scott stresses that the lack of these findings should not deter doctors from performing genetic testing for their patients with neurodevelopmental symptoms.

Children who don’t look like they have a genetic syndrome, but have these neurodevelopmental issues, could carry changes in this gene,” Scott said. “That’s why we should be doing genetic testing for all children who have developmental delay and intellectual disability.”

Providing answers and improving diagnosis

Documenting characteristics of disease genes like PAX5 not only can help expedite basic science and clinical research. According to Scott, the findings in this report provided long-awaited answers to the families in the study and will have an immediate impact for undiagnosed patients in genetics clinics.

As we discover new genes like PAX5, our diagnostic tests get better,” Scott said.

“From this point forward, diagnostic labs will start to check for changes in this gene. As geneticists, we are constantly reviewing older patient data to see if we can come up with new diagnoses thanks to discoveries like this one.”

Thanks to the discovery of genes like PAX5, scientists and physicians have a better understanding of a novel neurological condition, can provide answers to some undiagnosed patients and have an improved diagnostic ‘tool box’ when presented with a patient with undiagnosed neurodevelopmental issues.

Find all the details about this study in the journal Human Mutation.

Dr. Yoel Gofin, second-year medical genetics fellow in the Department of Molecular and Human Genetics at Baylor, is first author of the paper. Other authors at Baylor include Dr. Aliska M. Berry, Dr. Mahshid S. Azamian, Dr. Carlos A. Bacino, Dr. Seema R. Lalani and Jill A. Rosenfeld.

For a full list of authors and funding information, see the publication.

 

By Molly Chiu

 

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