Résumé
We describe a rare case of unilateral development of coxa vara secondary to metaphyseal dysostosis encountered in a 6-year-old boy. Family history and radiographic documentation revealed a 31-year-old father with a typical clinical history. Proximal femoral intertrochanteric valgus osteotomy and a revision cup [Allofit] have been performed for the child and his father respectively
Sujets)
Humains , Mâle , Enfant , Adulte , Dysostoses/imagerie diagnostique , Tête du fémur/malformations , Articulation de la hanche/malformations , Coxa vara/chirurgie , Dysostoses/chirurgie , Ostéotomie , Résultat thérapeutiqueRésumé
We report on a-6-months-old girl who manifested the phenotypic features of focal dermal hypoplasia. Significant limb deformities in connection with typical skin changes were documented. The family history had a high frequency of spontaneous abortions and male stillbirths. Male stillbirths are a landmark in favour of X-linked dominant pattern of inheritance. Despite the severe hand/foot deformities, the skull base and the tubular bones were sclerotic
Sujets)
Humains , Nourrisson , Femelle , Hypoplasie dermique en aires/complications , Hypoplasie dermique en aires/génétique , Maladies génétiques liées au chromosome X/génétique , Anomalies morphologiques congénitales des membres/imagerie diagnostique , Anomalies morphologiques congénitales des membres/complications , PhénotypeRésumé
We report the case of a girl-child who manifested the clinicoradiographic features of pseudorheumatoid arthritis. 3D-CT scan of the craniocervical junction showed distinctive features of dystopic type of os odontoideum. The report highlights the necessity to explore the craniocervical junction in patients with progressive pseudorheumatoid arthropathy