## Abstract We report on a father to daughter transmission of Barber–Say syndrome (BSS), a rare, congenital disorder characterized by severe generalized hypertrichosis, macrostomia, ocular telecanthus, bulbous nose and atrophic skin. These two cases further support the autosomal dominant inheritanc
Oral and dental abnormalities in Barber–Say syndrome
✍ Scribed by Fabiana Martins; Karem Lopez Ortega; Cybelle Hiraoka; Patricia Ricardo; Marina Magalhães
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 145 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
We report on a mother-to-son transmission of the Barber-Say syndrome, a finding that strongly supports dominant inheritance of this rare disorder. The characteristic facial changes, small ears, hirsutism, and redundant skin of our patients are consistent with the findings of five reported cases. The
We present a girl with lax, redundant skin, ectropion, bulbous nose, macrostomia, and absence of mammary glands. To our knowledge, she represents the fourth described case of Barber-Say Syndrome (BSS). BSS and ablepharon macrostomia syndrome (AMS) share common and distinctive clinical manifestations
In 1966 during a dental survey of four districts in Uganda-Acholi in the north, Bugisu in the east, and Kigezi and Tor0 i n the southwest -1169 Africans were examined. In the sample from Kigezi District 11.9% of the Bakiga tribe showed a form of dental mutilation consisting of the filing away of the