The Keutel syndrome (MIM 245150) is a rare autosomal recessive disorder, with only 13 patients reported thus far [reviewed by Teebi et al., 1998]. The recent identification of mutations in the calciumbinding matrix Gla protein in individuals with the Keutel syndrome has shed new light on the pathoge
Teebi hypertelorism syndrome with Tetralogy of Fallot
β Scribed by Nakagawa, Masao; Kondo, Masanori; Matsui, Akemi
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 8 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19980605)77:5<345::aid-ajmg1>3.0.co;2-m
No coin nor oath required. For personal study only.
β¦ Synopsis
A 34-month-old boy presented with clinical manifestations of Teebi hypertelorism syndrome including prominent forehead with frontal bossing, hypertelorism, exophthalmos due to shallow orbits, a short and broad nose with anteverted nares, small hands and feet with interdigital webbing, umbilical hernia, and shawl scrotum. In addition, he had previously undescribed manifestations including tetralogy of Fallot, bilateral inguinal testes, and bifid scrotum. His phenotypically normal mother showed splayed labiae majora during her pregnancy, a possible manifestation of the syndrome.
π SIMILAR VOLUMES
The retelling of the epic Welsh myth that is "certainly among the top 5 fantasy series of the twentieth century" (sfsite.com). The Mabinogion is to Welsh mythology what the tales of Zeus, Hera, and Apollo are to Greek myth. these tales constitute a powerful work of the imagination, ranking with Tok
From New York Times and USA Today bestselling author Kristen Proby... Fallon McCarthy has climbed the corporate ladder. She's had the office with the view, the staff, and the plaque on her door. The unexpected loss of her grandmother taught her that there's more to life than meetings and conference
Fallon McCarthy has climbed the corporate ladder. She's had the office with the view, the staff, and the plaque on her door. The unexpected loss of her grandmother taught her that there's more to life than meetings and conference calls, so she quit, and is happy to be a nomad, checking off items on
We report on a child with macrostomia, hypertelorism, atrophic skin, and severe hypertrichosis (Barber-Say Syndrome). To our knowledge this is the first case of this condition without ectropion; it is also a less severe phenotype than those reported previously.
The retelling of the epic Welsh myth that is "certainly among the top 5 fantasy series of the twentieth century" (sfsite.com). The Mabinogion is to Welsh mythology what the tales of Zeus, Hera, and Apollo are to Greek myth. these tales constitute a powerful work of the imagination, ranking with Toki