Novel variants in TNRC6B cause global developmental delay with speech and behavioral abnormalities, short stature, low body weight, caf é‐au‐lait spots, and metabolic abnormality

ConclusionThis study expands the genotypic and phenotypic spectrum of TNRC6B deficiency syndrome. Our findings indicate that patients with TNRC6B deficiency syndrome should be monitored for growth and metabolic problems and therapeutic strategies should be developed to address these problems. Our report also suggests the clinical diversity of TNRC6B deficiency syndrome.

Source: Molecular Genetics & Genomic Medicine - February 27, 2024 Category: Genetics & Stem Cells Authors: Qi Yang, Shan Ou, Xunzhao Zhou, Sheng Yi, Li Lin, Shang Yi, Shujie Zhang, Zailong Qin, Jingsi Luo Tags: ORIGINAL ARTICLE Source Type: research