Results 171 to 180 of about 9,046 (221)
Some of the next articles are maybe not open access.
Jansen's Metaphyseal Dysostosis
Pediatrics, 1976A case of Jansen's metaphyseal dysostosis, a rare disorder of endochondral ossification, is described. This is the first case in which the severe radiographic manifestations of this disease were detected at birth. Linear growth is significantly retarded at 2 years of age.
S L, Gordon +3 more
openaire +2 more sources
Pediatric Radiology, 1979
A 2 year old boy with humero-spinal dysostosis is described. This is the third case of this disease reported in the literature. Humero-spinal dysostosis is characterised radiologically by distal humeral bifurcation, elbow subluxation and coronal cleft vertebrae. Congenital, progressive heart disease, possibly with fatal outcome, is probably part of the
H, Cortina +5 more
openaire +2 more sources
A 2 year old boy with humero-spinal dysostosis is described. This is the third case of this disease reported in the literature. Humero-spinal dysostosis is characterised radiologically by distal humeral bifurcation, elbow subluxation and coronal cleft vertebrae. Congenital, progressive heart disease, possibly with fatal outcome, is probably part of the
H, Cortina +5 more
openaire +2 more sources
Radiology, 1973
A father and five children with a deformity of the thoracic cage alone are discussed. Each had a constricted, bell-shaped thorax with foreshortened and deformed ribs and a pectus excavatum deformity of the anterior chest wall. Clinically, there were repeated respiratory illnesses but no fatalities.
S E, Rabushka, L, Love, H I, Kadison
openaire +2 more sources
A father and five children with a deformity of the thoracic cage alone are discussed. Each had a constricted, bell-shaped thorax with foreshortened and deformed ribs and a pectus excavatum deformity of the anterior chest wall. Clinically, there were repeated respiratory illnesses but no fatalities.
S E, Rabushka, L, Love, H I, Kadison
openaire +2 more sources
Journal of Craniofacial Surgery, 1996
In six persons with mandibulofacial dysostosis, surgical correction of the anomaly was performed at different ages using different methods. In two persons between the ages of 7 and 9 years, correction of the zygomaticomaxillary region, using rib cartilage, was performed first.
R, Roncević, D, Roncević
openaire +2 more sources
In six persons with mandibulofacial dysostosis, surgical correction of the anomaly was performed at different ages using different methods. In two persons between the ages of 7 and 9 years, correction of the zygomaticomaxillary region, using rib cartilage, was performed first.
R, Roncević, D, Roncević
openaire +2 more sources
Acromelic Frontonasal Dysostosis
American Journal of Medical Genetics, 1999We report on 3 male and 2 female infants with acromelic frontonasal dysostosis. All 5 had a frontonasal malformation of the face and nasal clefting associated with striking symmetrical preaxial polysyndactyly of the feet and variable tibial hypoplasia. In contrast, the upper limbs were normal.
S F, Slaney +9 more
openaire +2 more sources
FAMILIAL CLEIDOCRANIAL DYSOSTOSIS (CLEIDAL DYSOSTOSIS)
American Journal of Diseases of Children, 1939A family with four members who have defective or missing clavicles is unusual, as only a few such families have been described. However, the condition is not a recent discovery. The first case of these defects was recorded as early as 1766 by Morand. 1 The first familial occurrence was reported over a century later by Cutter 2 (1870).
openaire +1 more source
The British Journal of Radiology, 1947
A Part from the abnormalities implied in the name of this condition, there are several associated anomalies that commonly occur. It is a rare disorder, congenital and nearly always hereditary, but the variety of its manifestations makes it most interesting.
openaire +2 more sources
A Part from the abnormalities implied in the name of this condition, there are several associated anomalies that commonly occur. It is a rare disorder, congenital and nearly always hereditary, but the variety of its manifestations makes it most interesting.
openaire +2 more sources