Article
ENT manifestations of Fraser syndrome.
The Journal of laryngology and otology - 1 Jan 1992
Ford G R, Irving R M, Jones N S, Bailey C M
Abstract excerpt
Fraser Syndrome is a rare autosomal recessive disorder (Gupta and Saxena, 1962; Smith, 1982). The most consistent feature is cryptophthalmos (hidden eye), but frequently abnormalities of the ears (meatal stenosis, dysplastic pinna), nose (hypoplastic notched nares, choanal stenosis or atresia), and larynx (glottic web, subglottic stenosis), as well as numerous other anomalies are encountered. We present four...
Topics
- Abnormalities, Multiple
- Child
- Child, Preschool
- Ear, External
- Eyelids
- Female
- Humans
- Larynx
- Male
- Nose
- Phenotype
- Syndrome