The Clinical Cases of Geleophysic Dysplasia: One Gene, Different Phenotypes.
Evgenia GlobaNataliya ZelinskaAndrew DauberPublished in: Case reports in endocrinology (2018)
Patients with severe dwarfism, skeletal anomalies, and other specific syndromic features (e.g., tracheal stenosis and cardiac valvulopathy) should undergo genetic testing to exclude acromelic dysplasia syndromes.