Co-segregation of Freiberg's infraction with a familial translocation t(5;7)(p13.3;p22.2) ascertained by a child with cri du chat syndrome and brachydactyly type A1B.

Abstract

The identification of chromosomal breakpoints in association with human abnormal phenotypes can enable elucidation of gene function. We report on epiphyseal aseptic necrosis of the lesser head of the second metatarsal bone, known as Freiberg's infraction (FI), in two female carriers of the apparently balanced t(5;7)(p13.3;p22.2) ascertained by a 16-year-old girl with cri-du-chat syndrome and unusual skeletal features in association with an unbalanced translocation der(5) t(5;7)(p13.3;p22.2). Mapping of the chromosome breakpoints using fluorescent in situ hybridization (FISH) narrowed them to the coding sequence of ADAMTS12 on chromosome 5p13.3 and SDK1 on 7p22.2. In addition, several skeletal abnormalities classified as brachydactyly type A1B (BDA1B) were present in the proband and in both carriers of t(5;7)(p13.3;p22.2), suggesting a potential role of ADAMTS12 in the development of the BDA1B observed in this family.

• Authors: Marta Myśliwiec, Barbara Panasiuk, Maria Dębiec-Rychter, Piotr Sebastian Iwanowski, Urszula Łebkowska, Beata Nowakowska, Anna Marcinkowska, Pawel Stankiewicz, Alina T Midro
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 167A Issue 2 Pg. 445-9 (Feb 2015) ISSN: 1552-4833 [Electronic] United States
• PMID: 25756154 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Topics

• Adolescent
• Brachydactyly (diagnosis, genetics)
• Child
• Chromosomes, Human, Pair 5
• Chromosomes, Human, Pair 7
• Cri-du-Chat Syndrome (diagnosis, genetics)
• Facies
• Fatal Outcome
• Female
• Humans
• Metatarsus (abnormalities)
• Osteochondritis (congenital, diagnosis, genetics)
• Phenotype
• Radiography
• Spine (abnormalities, diagnostic imaging)
• Translocation, Genetic