Zobrazeno 1 - 10
of 12
pro vyhledávání: '"H S, Hosalkar"'
Publikováno v:
Der Orthopade. 48(8)
The purpose of this review is to present the pros and cons as well as the surgical techniques of conventional implants used for fixation of slipped capital femoral epiphysis (SCFE). Worth mentioning are K‑wires, Hansson pins, transfixing screws, an
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :578-583
The association between vitamin-D-resistant rickets and linear sebaceous naevus syndrome is extremely rare. Only eight cases have been described in the English literature and in none were the skeletal aspects addressed. We present three new cases and
Publikováno v:
Journal of postgraduate medicine. 48(1)
Publikováno v:
Journal of postgraduate medicine. 47(4)
The Antley-Bixler syndrome is a rare multiple congenital anomaly with a high mortality rate. The characteristic manifestations include craniosynostosis, radiohumeral synostosis, midface hypoplasia, joint contractures and arachnodactyly. We report two
Publikováno v:
Journal of postgraduate medicine. 47(3)
Publikováno v:
Radiologic clinics of North America. 39(4)
Although a detailed, comprehensive look at pediatric orthopedists' use of imaging is beyond the scope of this article, we offer an orthopedist's perspective of the role imaging plays in the care of children with tumors, scoliosis, and trauma. Given t
Publikováno v:
Journal of postgraduate medicine. 46(4)
Cerebro-costo-mandibular syndrome (CCMS) is a rare multiple congenital anomaly with a low survival rate. There are few reports of long-term survival in this condition. We describe the findings and management of a 9-year-old survivor of CCMS, outline
Publikováno v:
Journal of postgraduate medicine. 45(3)
A common and conspicuous congenital hand anomaly, polydactyly commonly involves only the hand or the foot. Polydactyly involving both hands and feet is rare. We herewith report two cases of Crossed Polydactyly (Type I) and review the literature.
Publikováno v:
Journal of Postgraduate Medicine, Vol 45, Iss 4, Pp 123-4 (1999)
In view of the different modes of inheritance and the different prognoses of the two oro-facio-digital syndromes, type 1 and type 2, it is important to establish a correct diagnosis in these patients. A case of type II oro-facio-digital syndrome is b
Publikováno v:
Journal of Postgraduate Medicine, Vol 46, Iss 2, Pp 129-129 (2000)