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Congenital pseudarthrosis of the clavicle.
Pediatr Radiol
December 2009
Department of Radiology, Texas Scottish Rite Hospital for Children, Dallas, TX 75219, USA.
Background: Congenital pseudarthrosis is an uncommon anomaly poorly referred to in the pediatric literature.
Objective: To describe congenital pseudarthrosis in children. We discuss the presentation, clinical symptomatology, and treatment.
Hajdu-Cheney syndrome associated with serpentine fibulae and polycystic kidney disease.
Pediatr Radiol
January 2009
Department of Radiology, Texas Scottish Rite Hospital, 2222 Welborn St., Dallas, TX 75219, USA.
Six patients who presented with craniofacial anomalies, musculoskeletal anomalies including elongated and bowed (serpentine) fibulae, and polycystic kidneys are reported. This association of anomalies is referred to as serpentine fibula polycystic kidney syndrome (SFPKS) and is currently interpreted as a manifestation of Hajdu-Cheney syndrome (HCS). We report a new instance of this association of anomalies and review the clinical and radiographic features of HCS and of the reported cases of SFPKS.
View Article and Find Full Text PDFNeonatal subperiosteal cephalohematoma crossing a synostosed sagittal suture.
Pediatr Radiol
December 2007
Department of Radiology, Texas Scottish Rite Hospital, Dallas, TX 75219, USA.
A newborn boy, born at term by a spontaneous delivery, presented in the first day of life with a soft-tissue mass across a synostosed segment of the sagittal suture. In the following week the mass became better defined and showed peripheral calcifications consistent with a calcified subperiosteal hematoma.
View Article and Find Full Text PDFSagittal synostosis in X-linked hypophosphatemic rickets and related diseases.
Pediatr Radiol
August 2007
Department of Radiology, Texas Scottish Rite Hospital, 222 Welborn St., Dallas, TX 75219, USA.
Background: The recent observations of two new cases of X-linked hypophosphatemic rickets associated with premature closure of the sagittal suture prompted a review of similar cases seen in this institution.
Objectives: To review the clinical records and skull radiographs of 28 children with hypophosphatemic rickets in order to investigate the frequency and type of craniosynostosis and other cranial vault changes seen in these conditions and to review the literature for relevant findings.
Materials And Methods: Clinical and imaging records were reviewed on 28 patients with hypophosphatemic rickets, all younger than 18 years.
Lesions of the accessory parotid gland in children.
Pediatr Radiol
January 2006
Department of Radiology, Children's Medical Center, Dallas, TX, USA.
The accessory parotid gland, a little-known and seldom-mentioned anatomical variant, is a nodule of normal salivary tissue separate from the main parotid gland, located on the masseter muscle and connected to the Stensen duct at that level. It can be the site of both congenital and acquired lesions.
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