Lois J. Starr

Oct 11, 2024 | onlinelibrary.wiley.com | Stevin Lu |Lois J. Starr |Rachel Taylor |Anji T. Yetman

1 Introduction Turner syndrome (TS) is a relatively common genetic disorder characterized by complete or partial absence of an X chromosome in females (Cui et al. 2018). The co-morbid conditions associated with TS have been well characterized and include congenital cardiac, renal, and reproductive organ anomalies (Cui et al. 2018). Patients may also have a host of acquired conditions with potential for development of autoimmune, hepatic, neurologic, musculoskeletal, and cardiac disease (Cui et al.

Oct 1, 2024 | pericles.pericles-prod.literatumonline.com | Angela Lin |Lois J. Starr |Children's Nebraska |Kate Wears

REFERENCES , , , et al. 2012. “A Restrictedspectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhresyndrome.” American Journal of Human Genetics 90: 161–169. , , , et al. 2011. “Mutations at a Single Codon in Madhomology 2 Domain of SMAD4 Cause Myhre Syndrome.” Nature Genetics 44, no. 1: 85–88. https://www.nature.com/articles/ng.1016. , , , et al. 2022. “ Myhre Syndrome.” In GeneReviews®, edited by M. P. Adam, J. Feldman, G. M. Mirzaa, et al., 1993–2024.