Cranio‐Metaphyseal Dysplasia (Report of 3 cases ‐ two infants and one adult)

Australasian Radiology

Volumn 32, Issue 2, 1988, Pages 257-262

  COLAVITA, N ^a   KOZLOWSKI, K ^b   SPRAGUE, P ^c  

^a CATHOLIC UNIVERSITY   (Italy)

^b CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^c PRINCESS MARGARET HOSPITAL FOR CHILDREN   (Australia)

Author keywords

Cranial nerve dysfunction; Cranio metaphyseal dysplasia; Sclerotic bone dysplasia

Indexed keywords

RADIOISOTOPE;

ADULT; BONE RADIOGRAPHY; CASE REPORT; CRANIOMETAPHYSEAL DYSPLASIA; FEMALE; HEREDITY; HUMAN; INFANT; MALE; SKULL RADIOGRAPHY;

EID: 0023806968     PISSN: 00048461     EISSN: 14401673     Source Type: Journal    
DOI: 10.1111/j.1440-1673.1988.tb02733.x     Document Type: Article

References (12)

1. Craniometaphyseal Dysplasia ‐ Variability of Expres sion within a large Family
2. Die Metaphysare Dysplasie ‐ Morbus Pyle
3. Genetic Craniotubular Bone Dysplasias and Hyperostoses
4. La Dysplasie Cranio‐Metaphysaire
5. Otorhinologische Gesichtspunkte bei der Kraniometaphysaren Dysplasie (Pyle‐Syndrome)
6. Craniometaphyseal Dysplasia (Pyle's Disease)Autosomal Dominant Inheritance in a Large Kindred
7. Cranial Metaphyseal Dysplasia
8. Die Craniometaphysare Dysplasie (Pyle‐Syndrome) ‐ Bericht uber 4 Falle aus einer Familie
9. Radiology of the Autosomal Dominant Form of Craniometaphyseal Dysplasia
10. Die Kraniometaphysare Dysplasie (Pyle)
11. A Case of Autosomal Recessive Form of Cranio‐metaphyseal Dysplasia with Unusual Features and with Bone Fragility