BBBG syndrome or opitz syndrome: New family
β Scribed by Verloes, Alain ;Le Merrer, Martine ;Briard, Marie-Louise
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 409 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
We report on four unrelated cases of an Opitz trigonocephaly (C)-like syndrome with a highly characteristic combination of facial anomalies including prominent metopic suture, exophthalmos, hypertelorism, cleft lip and palate, flexion deformities of the upper limbs and multiple other anomalies. We a
## To the Editor: The Opitz or BBBG syndrome is an autosomal dominant disorder characterized by facial anomalies and multiple congenital abnormalities. Recent evidence would suggest that the Opitz and BBB syndromes form a spectrum of the same condition Verloes et al., 19891 and it has been sugges