✦ LIBER ✦

A sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome

✍ Scribed by Pelias, Mary Z. ;Superneau, Duane W. ;Thurmon, Theodore F. ;Opitz, John M.

Publisher: John Wiley and Sons
Year: 1981
Tongue: English
Weight: 393 KB
Volume: 10
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320100206

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Baller-Gerold syndrome: An 11th case of

Baller-Gerold syndrome: An 11th case of craniosynostosis and radial aplasia

✍ Boudreaux, Jeanne M. ;Colon, Marc A. ;Lorusso, Giovanni D. ;Parro, Elizabeth A. 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 421 KB 👁 1 views

We report on a patient with craniosynostosis, left radius aplasia, right radius hypoplasia, and other congenital anomalies. This is the 11th reported case of the Baller-Gerold syndrome. Autosomal recessive inheritance of this syndrome is suggested by evidence of probable parental consanguinity.

TWIST gene mutation in a patient with ra

TWIST gene mutation in a patient with radial aplasia and craniosynostosis: Further evidence for heterogeneity of Baller-Gerold syndrome

✍ Gripp, Karen W.; Stolle, Catherine A.; Celle, Livija; McDonald-McGinn, Donna M.; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 44 KB 👁 2 views

The term Baller-Gerold syndrome was coined by Cohen [1979: Birth Defects 15(5B): 13-63] to designate the phenotype of craniosynostosis and radial aplasia. It is thought to be a rare autosomal recessive condition, which, in some patients, presents with additional abnormalities, such as polymicrogyria