March 16, 2020
Cameron’s New Way Forward After Rare Disease Diagnoses
Cameron Kaipainen and his parents spent years searching for explanations to his ongoing and confusing medical problems. It wasn’t until arriving at Mayo Clinic in Arizona that the true nature of Cameron’s condition was uncovered, giving the family the priceless gift of knowledge.
Tags: 7q11.23 duplication syndrome, Clinical Genomics, Dr. Bernard Bendok, Dr. Radhika Dhamija, Schwannoma, Schwannomatosis
February 10, 2020
Careful Evaluation, Genetic Testing Offer a New Path Forward
Diagnosed with multiple sclerosis, Maureen Jessen, always wondered why the disease affected her so differently than it did others. Doctor after doctor told her that MS was likely causing her symptoms, so she believed them. Mayo Clinic specialists, however, gave Maureen new insight into her illness — one that had nothing to do with MS.
Tags: Center for Individualized Medicine, Center for Multiple Sclerosis and Autoimmune Neurology, Clinical Genomics, Dr. Cristina Valencia Sanchez, Dr. Dean Wingerchuk, Dr. Radhika Dhamija
February 13, 2019
Comprehensive Care Makes for a Brighter Future
When Stephanie Van Doren came to Mayo Clinic, she never expected to learn she had a genetic defect that raised her risk for a potentially fatal heart condition. But thanks to her physician’s all-inclusive approach, Stephanie and her family now have information they need to live life to the fullest.
Tags: Clinical Genomics, Dr. Timothy Woodward, Eosinophilic esophagitis, Genetic testing
February 13, 2018
Genetic Sleuths Dig Deep to Identify a Young Boy’s Rare Condition
When Karter Malcomson was born, his care team knew it was likely he had a genetic disorder. But a clear diagnosis was elusive. That’s when the functional genomics team at Mayo Clinic’s Center for Individualized Medicine went to work. And they didn’t give up until they had an answer.
Tags: Center for Individualized Medicine, Clinical Genomics, Dr. Charu Kaiwar, Dr. Filippo Pinto e Vairo, Dr. Margot Cousin, Dr. Nicole Boczek, Dr. Pavel Pichurin
October 5, 2017
Teen Navigates Ehlers-Danlos Syndrome With the Help of Clinical Genomics
After years of dealing with mysterious symptoms, Nicole Rickert was diagnosed with Ehlers-Danlos syndrome. Now she’s working with her team at Mayo Clinic to get the care she needs to move forward into a healthy future.
Tags: Clinical Genomics, Dr. Radhika Dhamija, Ehlers-Danlos Syndrome
March 1, 2017
After Years of Pain, a Clear Diagnosis Restores a Teen’s Life
Written by Sanan Malkadjian I was only 14 at the time. I would be ashamed of myself because of how often my stomach hurt. It came to a point where no one would believe the excruciating pain I was facing. This was pain unlike no other. My doctors here in Michigan would blame one another. […]
Tags: Clinical Genomics, Dr. Magnus Halland, Familial Mediterranean Fever, Gastroenterology