This week’s roundup features research reinforcing the need for better universal surveillance for developmental delays and increased access to early intervention. This and more In The News.
Knowing the causative genes for osteoporosis may later open the door to more effective treatments. Research by Struan Grant, PhD, and Andrew Wells, PhD.
New preclinical findings from extensive cell and animal studies suggest that a drug already used for a rare kidney disease could benefit patients with some mitochondrial disorders—complex conditions with severe energy deficiency for which no proven effective treatments exist. Future clinical research is needed to explore whether the drug, cysteamine bitartrate, will meaningfully benefit patients.
This week in research news: teasing out genetic clues across the skeleton, a "missing mutation" in infant epilepsy, and studying soy-based baby formulas.
Supporting a diverse community of investigators and clinicians in groundbreaking basic, translational, and clinical research in mitochondrial biology and disease.