Acromesomelic dysplasia: Radiologic, clinical, and pathological study
✍ Scribed by del Moral, Rafael Fernández ;Jiménez, José M. Santolaya ;González, José I. Rodríguez ;Vicario, Ricardo Franco
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 479 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract We report on 14 fetuses from 10 families with the autosomal recessive syndrome of proliferative vasculopathy and hydranencephaly–hydrocephaly (Fowler syndrome). In four families sibs were affected and in six the parents were consanguineous. Antenatal ultrasonography showed hydrocephaly
Background. Giant cell tumors (GCT) usually involve the epiphyses of long bones and only rarely involve the metaphysis or diaphysis without epiphyseal extension. Methods. This report presents the clinical and pathologic features of 14 patients with metaphyseal and diaphyseal GCT. Of these tumors, 1