Baller‐Gerold syndrome associated with congenital hydrocephalus Journal Articles

abstract

• AbstractWe present a new case of the Baller‐Gerold syndrome (BGS) in an infant with prenatally apparent severe hydrocephalus, growth retardation, and cardiac and limb abnormalities detected by ultrasound at 26 weeks of gestational age. Subsequent survival to term and neonatal examination confirmed an unsuspected diagnosis of BGS.

authors

• Lewis, ME Suzanne
• Rosenbaum, Peter L
• Paes, Bosco

status

• published 

publication date

• September 1991

has subject area

• 0604 Genetics (FoR)
• 1103 Clinical Sciences (FoR)
• Abnormalities, Multiple (MeSH)
• Brain (MeSH)
• Female (MeSH)
• Humans (MeSH)
• Hydrocephalus (MeSH)
• Infant, Newborn (MeSH)
• Prenatal Diagnosis (MeSH)
• Syndrome (MeSH)
• Tomography, X-Ray Computed (MeSH)
• Ultrasonography (MeSH)

published in

• American Journal of Medical Genetics, Part A  Journal

keywords

• Abnormalities, Multiple
• Brain
• Female
• Humans
• Hydrocephalus
• Infant, Newborn
• Prenatal Diagnosis
• Syndrome
• Tomography, X-Ray Computed
• Ultrasonography

Digital Object Identifier (DOI)

• 10.1002/ajmg.1320400312

PubMed ID

• 1951434

start page

• 307

end page

• 310

volume

• 40

issue

• 3