Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY
- PMID: 32243688
- DOI: 10.1002/ajmg.a.61578
Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY
Abstract
49,XXXXY is the rarest X and Y chromosomal variation, with an incidence of 1 in 80,000-100,000 live male births and has been associated with numerous musculoskeletal abnormalities. Data was collected from an international cohort of boys with 49,XXXXY over 10 years. Children were evaluated by a multidisciplinary team consisting of a pediatric orthopedist, a neurogeneticist, a neurodevelopmentalist, and two physical therapists. Increased rates of torticollis (32.4%), hamstring tightness (42%), radioulnar synostosis (67.6%), pes planus (65.2%), and other foot abnormalities (86.9%) were observed. Several anomalies increased with age, specifically hamstring tightness, kyphosis, and scoliosis. The elucidation of the orthopedic profile of this population is necessary in order to provide healthcare providers with current medical information. This research further supports the necessity for the comprehensive multidisciplinary treatment of boys with 49,XXXXY.
Keywords: 49,XXXXY; X and Y chromosomal variations; musculoskeletal health; orthopedics; physical therapy; sex chromosome abnormalities and aneuploidies.
© 2020 Wiley Periodicals, Inc.
References
REFERENCES
-
- Academy of Pediatric Physical Therapy Fact Sheet. The Role and Scope of Pediatric Physical Therapy in Fitness, Wellness, Health Promotion, and Prevention. (2012).
-
- Argun, M., Akin, M. A., Kurtoglu, S., Sarıca, D., Özyurt, A., Pamukcu, Ö., & Baykan, A. (2015). Congenital heart disease in an infant with 49,XXXXY syndrome. The Journal of Current Pediatrics, 13(1), 63-67. https://doi.org/10.4274/jcp.88597
-
- Atik, T., Cogulu, O., & Ozkinay, F. (2015). A rare sex chromosome aneuploidy: 48, xxyy syndrome. Türk Pediatri Arşivi. doi: https://doi.org/10.5152/turkpediatriars.2015.1155
-
- Burgemeister, A. L., Daumiller, E., Bois, G. D., Graul-Neumann, L. M., Köhler, B., Knecht, S., … Zirn, B. (2019). Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum. European Journal of Medical Genetics, 62(3), 210-216. https://doi.org/10.1016/j.ejmg.2018.07.016
-
- Carenzio, G., Carlisi, E., Morani, I., Tinelli, C., Barak, M., Bejor, M., & Dalla Toffola, E. (2015). Early rehabilitation treatment in newborns with congenital muscular torticollis. European Journal of Physical Rehabilitative Medicine, 51(5), 539-545.
MeSH terms
Supplementary concepts
LinkOut - more resources
Full Text Sources
Medical