Walker-Warburg syndrome.
Publication
, Journal Article
Rhodes, RE; Hatten, HP; Ellington, KS
Published in: AJNR Am J Neuroradiol
1992
The Walker-Warburg syndrome (WWS) is a rare autosomal recessive disorder characterized by lissencephaly, cerebellar and retinal malformations, and congenital muscular dystrophy. We report a new case of WWS identified with the aid of cranial MR and briefly review the radiologic findings of this lethal syndrome.
Duke Scholars
Published In
AJNR Am J Neuroradiol
ISSN
0195-6108
Publication Date
1992
Volume
13
Issue
1
Start / End Page
123 / 126
Location
United States
Related Subject Headings
- Syndrome
- Retina
- Nuclear Medicine & Medical Imaging
- Muscular Dystrophies
- Male
- Magnetic Resonance Imaging
- Infant, Newborn
- Humans
- Cerebral Cortex
- Cerebellum
Citation
APA
Chicago
ICMJE
MLA
NLM
Rhodes, R. E., Hatten, H. P., & Ellington, K. S. (1992). Walker-Warburg syndrome. AJNR Am J Neuroradiol, 13(1), 123–126.
Rhodes, R. E., H. P. Hatten, and K. S. Ellington. “Walker-Warburg syndrome.” AJNR Am J Neuroradiol 13, no. 1 (1992): 123–26.
Rhodes RE, Hatten HP, Ellington KS. Walker-Warburg syndrome. AJNR Am J Neuroradiol. 1992;13(1):123–6.
Rhodes, R. E., et al. “Walker-Warburg syndrome.” AJNR Am J Neuroradiol, vol. 13, no. 1, 1992, pp. 123–26.
Rhodes RE, Hatten HP, Ellington KS. Walker-Warburg syndrome. AJNR Am J Neuroradiol. 1992;13(1):123–126.
Published In
AJNR Am J Neuroradiol
ISSN
0195-6108
Publication Date
1992
Volume
13
Issue
1
Start / End Page
123 / 126
Location
United States
Related Subject Headings
- Syndrome
- Retina
- Nuclear Medicine & Medical Imaging
- Muscular Dystrophies
- Male
- Magnetic Resonance Imaging
- Infant, Newborn
- Humans
- Cerebral Cortex
- Cerebellum