Clin Genet. 1980 Feb;17(2):161-6.

Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome.

Abstract

A new case of the Baller-Gerold syndrome is described in a 6 1/2-year-old, black male who presented at birth with bilateral synostoses of the coronal and lambdoidal sutures, bilateral radial aplasia, vertebral anomalies and genito-urinary malformations. The parents and siblings were unaffected, and there was no history of consanguinity. A review of the history and physical findings in our patient and in the four other patients previously reported in the literature is provided, with a discussion on pathogenesis, prognosis and the possible autosomal recessive mode of inheritance of the syndrome.

PMID:: 7363501; [PubMed - indexed for MEDLINE]

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TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome. [Am J Med Genet. 1999]
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome.
Gripp KW, Stolle CA, Celle L, McDonald-McGinn DM, Whitaker LA, Zackai EH. Am J Med Genet. 1999 Jan 15; 82(2):170-6.
Review Baller-Gerold syndrome: an 11th case of craniosynostosis and radial aplasia. [Am J Med Genet. 1990]
Review Baller-Gerold syndrome: an 11th case of craniosynostosis and radial aplasia.
Boudreaux JM, Colon MA, Lorusso GD, Parro EA, Pelias MZ. Am J Med Genet. 1990 Dec; 37(4):447-50.
Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome. [Am J Med Genet. 1981]
Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome.
Pelias MZ, Superneau DW, Thurmon TF. Am J Med Genet. 1981; 10(2):133-9.
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Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia).
Galea P, Tolmie JL. J Med Genet. 1990 Dec; 27(12):784-7.
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Review Another TWIST on Baller-Gerold syndrome.
Seto ML, Lee SJ, Sze RW, Cunningham ML. Am J Med Genet. 2001 Dec 15; 104(4):323-30.

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Cited by 5 PubMed Central articles

Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. [J Med Genet. 2006]
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene.
Van Maldergem L, Siitonen HA, Jalkh N, Chouery E, De Roy M, Delague V, Muenke M, Jabs EW, Cai J, Wang LL, et al. J Med Genet. 2006 Feb; 43(2):148-52. Epub 2005 Jun 17.
Review Baller-Gerold syndrome associated with congenital portal venous malformation. [J Med Genet. 1998]
Review Baller-Gerold syndrome associated with congenital portal venous malformation.
Savarirayan R, Tomlinson P, Thompson E. J Med Genet. 1998 Sep; 35(9):767-9.
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome. [J Med Genet. 1990]
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome.
Huson SM, Rodgers CS, Hall CM, Winter RM. J Med Genet. 1990 Jun; 27(6):371-5.

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Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome.
Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome.
Clin Genet. 1980 Feb ;17(2):161-6.

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Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome.

Abstract

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Cited by 5 PubMed Central articles

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