Barth syndrome is caused by a mutation in the tafazzin gene, which results in reduced cardiolipin levels, a phospholipid that plays a major role in mitochondrial function. The disease is characterized ...

But Devin was born with Barth Syndrome, a rare genetic condition that impacts 1 in 300,000 to 400,000 people. At nine weeks old, he underwent his first heart transplant. "When they did that ...

To manage this experience, often called empty nest syndrome, you may need some lifestyle changes or professional help. Share on Pinterest Brat Co/Stocksy United The post-parental stage — which ...

Gary Raymond Barth, who taught mathematics at Concordia Preparatory School for 40 years, died of heart disease Feb. 18 at The Johns Hopkins Hospital. He was 67 and lived in Towson. Born in ...

The FDA is expected to decide on treatments for dry eye disease, neuroendocrine tumors, chronic spontaneous urticaria, Barth syndrome, and migraine. Reproxalap, a first-in-class small-molecule ...

What is lower crossed syndrome? If you’ve been told that you have lower crossed syndrome (LCS), you might wonder what this condition is, what causes it, and how it is treated. Lower crossed ...

Kaleb Stephen Barth, 24, of State College, passed away at home on Saturday, March 1, 2025. Arrangements are under the direction of Wetzler Funeral Service, Inc. in Bellefonte.

Barth syndrome (BTHS) is a rare genetic disorder due to mutations in the TAFAZZIN gene, leading to impaired maturation of cardiolipin and thereby adversely affecting mitochondrial function and energy ...

Finally, we have begun to explore the chromatin-related genome-wide effects of UBE3A dysregulation in human brain and neurons. We previously observed that elevated UBE3A in Dup15q syndrome had ...