Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group.

Abstract

Roberts syndrome (RS) is a rare autosomal recessive disorder characterized by heterogeneous clinical features, the most notable being tetraphocomelia, cleft lip, and cleft palate. Cells derived from most RS patients exhibit abnormal cytogenetic and cellular phenotypes that include the premature separation of para- and pericentromeric heterochromatin visible on C-banded metaphase chromosomes, a phenomenon referred to as heterochromatic splaying. Previously, it was shown that these abnormal phenotypes can be complemented following somatic cell hybridization between RS cells and control cells. In the current study, a permanent cell line was established from a new RS patient with a more severe phenotype than represented by previously established cells in culture. With a newly developed assay designed to facilitate rapid evaluation of in vitro complementation, we assigned this new patient to the same genetic complementation group defined by other, less severely affected patients. The results demonstrate that a single complementation group defines RS patients with heterochromatic splaying regardless of clinical severity.

• Authors: L D McDaniel, R Prueitt, L C Probst, K S Wilson, D Tomkins, G N Wilson, R A Schultz
• Journal: American journal of medical genetics (Am J Med Genet) Vol. 93 Issue 3 Pg. 223-9 (Jul 31 2000) ISSN: 0148-7299 [Print] United States
• PMID: 10925387 (Publication Type: Case Reports, Journal Article)

Topics

• Abnormalities, Multiple (classification, diagnosis, genetics)
• Arm (abnormalities)
• Cell Line
• Chromosome Banding
• Cleft Lip (genetics)
• Cleft Palate (genetics)
• Genes, Recessive
• Genetic Complementation Test (methods)
• Humans
• Infant
• Karyotyping
• Leg (abnormalities)
• Male
• Models, Genetic
• Phenotype
• Syndrome