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Contiguous Gene Deletion within Chromosome Arm 10q Is Associated with Juvenile Polyposis of Infancy, Reflecting Cooperation between the BMPR1A and PTEN Tumor-Suppressor Genes
- Source :
- The American Journal of Human Genetics. 78:1066-1074
- Publication Year :
- 2006
- Publisher :
- Elsevier BV, 2006.
-
Abstract
- We describe four unrelated children who were referred to two tertiary referral medical genetics units between 1991 and 2005 and who are affected with juvenile polyposis of infancy. We show that these children are heterozygous for a germline deletion encompassing two contiguous genes, PTEN and BMPR1A. We hypothesize that juvenile polyposis of infancy is caused by the deletion of these two genes and that the severity of the disease reflects cooperation between these two tumor-suppressor genes.
- Subjects :
- Male
medicine.medical_specialty
Tumor suppressor gene
Molecular Sequence Data
Biology
Contiguous gene syndrome
Germline
Germline mutation
Report
Genetics
medicine
Humans
PTEN
Genes, Tumor Suppressor
Genetics(clinical)
Juvenile polyposis syndrome
Letter to the Editor
Bone Morphogenetic Protein Receptors, Type I
Germ-Line Mutation
Genetics (clinical)
Base Sequence
Chromosomes, Human, Pair 10
Intestinal Polyposis
PTEN Phosphohydrolase
Infant
medicine.disease
BMPR1A
Child, Preschool
biology.protein
Medical genetics
Gene Deletion
Subjects
Details
- ISSN :
- 00029297
- Volume :
- 78
- Database :
- OpenAIRE
- Journal :
- The American Journal of Human Genetics
- Accession number :
- edsair.doi.dedup.....ea771392133b3377738caff70df79a81
- Full Text :
- https://doi.org/10.1086/504301