Baylor Researchers Expand Diagnosis for Xia-Gibbs Syndrome
August 19, 2021
August 19, 2021
HOUSTON, Texas, Aug. 19 (TNSJou) -- The Baylor College of Medicine issued the following news:
Researchers at the Human Genome Sequencing Center at Baylor College of Medicine have validated a new type of genetic mutation that causes Xia-Gibbs Syndrome (XGS), a rare genetic disorder that results in severe developmental delay, sleep apnea, delayed speech and upper body weakness. Their findings are published in the journal Human Genetics and Genomics Advances.
Discovered in . . .
Researchers at the Human Genome Sequencing Center at Baylor College of Medicine have validated a new type of genetic mutation that causes Xia-Gibbs Syndrome (XGS), a rare genetic disorder that results in severe developmental delay, sleep apnea, delayed speech and upper body weakness. Their findings are published in the journal Human Genetics and Genomics Advances.
Discovered in . . .