Microcephalic osteodysplastic primordial dwarfism type II.
We report a child with osteodysplastic primordial dwarfism type II. The literature is reviewed.
Bone and Bones↗
Biomedical subjects
W Lytle
Publications and source records attributed to W Lytle.
Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?
We report two sibs of consanguineous parents with multiple congenital abnormalities which include prenatal and postnatal growth retardation, anterior segment defects of the eye, arachnodactyly with other skeletal abnormalities, congenital heart disease and early lethality. We think this constellation of anomalies may represent a previously undescribed syndrome. There are some similarities to Michels syndrome from which it should be differentiated.
Abnormalities, Multiple↗
Otospondylomegaepiphyseal dysplasia: report of three sibs and review of the literature.
We report three sibs with clinical and radiological features of otospondylomegaepiphyseal (OSMED) syndrome. The literature is reviewed.
Abnormalities, Multiple↗