Article
Evidence of central nervous system involvement in Watson syndrome.
Pediatric neurology - 1 Apr 1995
Leão M, da Silva M L
Abstract excerpt
In 1967, Watson described 3 families with an autosomal dominant condition characterized by pulmonary valvular stenosis, café-au-lait sports, and short stature. Presumed hamartomatous lesions have been observed in neurofibromatosis type I, but they were not reported to date in Watson syndrome. We...
Topics
- Brain
- Brain Neoplasms
- Child
- Chromosome Aberrations
- Chromosome Disorders
- Genes, Dominant
- Humans
- Magnetic Resonance Imaging
- Male
- Neurofibromatosis 1
- Phenotype
- Pulmonary Valve Stenosis
- Syndrome
