Omodysplasia
Overview
Affiliations
Three cases of a new congenital bone disorder associating facial anomalies (depressed nasal bridge, broad base of the nose, long philtrum) with short humeri. The complex skeletal abnormalities consist of a defect of growth of the distal end of the humerus, a hypoplastic everted condyle, an upper radioulnar diastasis, and a anterolateral dislocation of the head of the radius. The condition is dominantly inherited. Two other cases with the same facial anomalies and osteoarticular abnormalities of the upper limbs are described. These cases also showed a severe micromelic dwarfism due to shortness of the long bones, particularly the femora. The present authors consider that these represent variable expressivity of the same disorder and propose that this condition be called omodysplasia (from the Greek term for humerus).
Non-canonical WNT5A-ROR signaling: New perspectives on an ancient developmental pathway.
Konopelski Snavely S, Srinivasan S, Dreyer C, Tan J, Carraway 3rd K, Henry Ho H Curr Top Dev Biol. 2023; 153:195-227.
PMID: 36967195 PMC: 11042798. DOI: 10.1016/bs.ctdb.2023.01.009.
Dominant omodysplasia-A sporadic case-A new case report and review of the literature.
Arabzadeh A, Baghianimoghadam B, Nabian M, Fallah Y, Ebrahimnasab M Clin Case Rep. 2022; 10(8):e6187.
PMID: 35937024 PMC: 9347672. DOI: 10.1002/ccr3.6187.
Zhang C, Jolly A, Shayota B, Mazzeu J, Du H, Dawood M HGG Adv. 2022; 3(1):100074.
PMID: 35047859 PMC: 8756549. DOI: 10.1016/j.xhgg.2021.100074.
Novel Clinical and Radiological Findings in a Family with Autosomal Recessive Omodysplasia.
Bayat A, Duno M, Kirchhoff M, Jorgensen F, Nishimura G, Hove H Mol Syndromol. 2020; 11(2):83-89.
PMID: 32655339 PMC: 7325126. DOI: 10.1159/000506384.
Two unrelated patients with autosomal dominant omodysplasia and mutations.
Warren H, Louie R, Friez M, Frias J, Leroy J, Spranger J Clin Case Rep. 2018; 6(11):2252-2255.
PMID: 30455931 PMC: 6230601. DOI: 10.1002/ccr3.1818.