Cerebellomedullary compression in recessive craniometaphyseal dysplasia

Author:

Boltshauser E.,Schmitt B.,Wichmann W.,Valavanis A.,Sailer H.,Yonekawa Y.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Radiology Nuclear Medicine and imaging

Reference8 articles.

1. McKusick VA (1992) Mendelian inheritance in man, 10th edn Johns Hopkins University Press, Baltimore

2. Gorlin RJ (1994) Craniotubular bone disorders. Pediatr Radiol 24: 392–406

3. Schroeder C, Quirin A, Oppermann HC, Oldigs HD (1992) Craniometaphysaere Dysplasie — charakteristische Roentgenbefunde. Klin Paediatr 204: 174–176

4. Scott RM, Wolpert SM, Pashayan HM (1983) Progressive optic nerve compression in craniometaphyseal dysplasia. In: Humphreys RP (ed) Concepts in pediatric neurosurgery, 4. Karger, Basel, pp 208–218

5. Puliafito CA, Wray SH, Murray JE, Boger WP (1981) Optic atrophy and visual loss in craniometaphyseal dysplasia. Am J Ophthalmol 92: 696–701

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