Osteogenesis imperfecta: Report of a case

Osteogénesis imperfecta: Reporte de un caso

Main Article Content

José Joaquín Suárez
Roy Riascos
José Mary González

Abstract

Osteogenesis imperfecta or Lobstein's disease is a deforming bone disorder in which the genes that make up collagen are affected. It is characterized clinically by the presence of deformed bones with multiple pathological fractures, blue scleras and hearing loss. It is divided into two main groups, the lethal or congenital form and the late one. We present an interesting case of the latter that was diagnosed by intrauterine ultrasound.

Downloads

Download data is not yet available.

Article Details

References

1. Diagnostic ultrasound; Karoll M. Rumack, 2a ed, Vol 2; pgs: 2114-2116, 1223.

2. Pediatric X-Ray Diagnosis; John Caffey. 5' ed; pgs 853-857.

3 Imagin of Newborn, infant, and young child; Leonard E. Swischuck, 4' ed; pgs 802 —804.

4. Roentgen diagnosis of disease born; Jack Edeinken, Hodes. Pags: 149-159. Munoz C, Fillyra , Golbus MS. Osteogenesis imperfecta Tipo II: Prenatal sonographic diagnosis. Radiology 1990; 174: 181-185

5.Goldman AB, Davison D, Pavlov H, et all. "popcom"calcifications: a prognostic sign in osteogenesis imperfecta. Radiology 1980; 136: 351-358.

Citado por