Langer-Giedion syndrome with 8q23.1-q24.12 deletion diagnosed by comparative genomic hybridization

The Langer-Giedion syndrome, also known as trichorhinophalangeal syndrome type II, is a hereditary multisystemic disease part of the group of contiguous gene deletion syndromes. The cause of this syndrome is a heterozygous deletion that involves the chromosomal region 8q23.3-q24.11 and mainly affects genes TRPS1, RAD21, and EXT1. This syndrome is characterized by the presence of multiple osteochondromas in limbs, hypertrichosis, and facial phenotype that includes sparse scalp hair, large laterally protruding ears, a long nose with a bulbous tip. We report the case of a Colorribian patient with finding of an 8q23.1-q24.12 deletionby comparative genomic hybridization array technique and classical clinical findings, being the first case reported in Colorribia.