Chromosome 1, deletion q21 q25
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Raviteja Guddeti, M.B.B.S.[3]
Overview
A rare chromosomal disorder where deletion of a portion of chromosome 1 results in various abnormalities such as retarded fetal growth, facial anomalies, osteoporosis, mental retardation and hearing loss.[1]
==References==