The syndrome of anosmia with hypogonadotropic hypogonadism: A genetic study of 18 new families and a review
β Scribed by White, Beverly J. ;Rogol, Alan D. ;Brown, Kenneth S. ;Lieblich, Jeffrey M. ;Rosen, Saul W. ;Opitz, John M.
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 999 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The Marshall syndrome is an autosomal dominant trait comprising ocular abnormalities, sensorineural hearing loss, craniofacial anomalies, and anhidrotic ectodermal dysplasia. To our knowledge, only seven additional multigenerational families have been reported since the initial description of the di
Blau syndrome (MK186580) comprises granulomatous arthritis, iritis, and skin rash, and is an autosomal-dominant trait with variable expressivity. So far it was described in 5 families. We report on a sixth family with severe progression of eye involvement and discuss the nosology with similar diseas
Recently, Shanske, et al. [1997] reported central nervous system anomalies in Seckel syndrome. We described what we thought to be the seventh instance of affected sibs born to normal parents and only the second family in which consanguinity had occurred. Imaging studies in our patient showed dysgen