الملخص
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
الموضوعات
Humans , Male , Child , Adult , Dysostoses/diagnostic imaging , Femur Head/abnormalities , Hip Joint/abnormalities , Coxa Vara/surgery , Dysostoses/surgery , Osteotomy , Treatment Outcomeالملخص
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
الموضوعات
Humans , Infant , Female , Focal Dermal Hypoplasia/complications , Focal Dermal Hypoplasia/genetics , Genetic Diseases, X-Linked/genetics , Limb Deformities, Congenital/diagnostic imaging , Limb Deformities, Congenital/complications , Phenotypeالملخص
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