Deficient knowledge in adult Turner syndrome care as an incentive to found Turner centers in Germany
- PMID: 31627185
- PMCID: PMC6865863
- DOI: 10.1530/EC-19-0418
Deficient knowledge in adult Turner syndrome care as an incentive to found Turner centers in Germany
Abstract
Objective: Turner syndrome (TS) is characterized by the complete or partial loss of the second sex chromosome and associated with a wide range of clinical manifestations. We aimed to assess the medical care of adult patients with TS in Germany.
Design: Retrospective multicenter observational study.
Methods: Data were collected from medical records of 258 women with TS treated between 2001 and 2017 in five non-university endocrinologic centers in Germany.
Results: Mean age was 29.8 ± 11.6 years, mean height 152 ± 7.7 cm, and mean BMI 26.6 ± 6.3 kg/m2. The karyotype was known in 50% of patients. Information on cholesterol state, liver enzymes, and thyroid status was available in 81-98% of women with TS; autoimmune thyroiditis was diagnosed in 37%. Echocardiography was performed in 42% and cardiac MRI in 8.5%, resulting in a diagnosis of cardiovascular disorder in 28%. Data on growth hormone therapy were available for 40 patients (15%) and data concerning menarche in 157 patients (61%).
Conclusion: In 258 women with TS, retrospective analysis of healthcare data indicated that medical management was focused on endocrine manifestations. Further significant clinical features including cardiovascular disease, renal malformation, liver involvement, autoimmune diseases, hearing loss, and osteoporosis were only marginally if at all considered. Based on this evaluation and in accordance with recent guidelines, we compiled a documentation form facilitating the transition from pediatric to adult care and further medical management of TS patients. The foundation of Turner Centers in March 2019 will improve the treatment of TS women in Germany.
Keywords: Turner centers; Turner syndrome; adult height; cardiovascular involvement; medical care.
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References
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- Ranke MB, Partsch CJ, Lindberg A, Dorr HG, Bettendorf M, Hauffa BP, Schwarz HP, Mehls O, Sander S, Stahnke N, et al. Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU follow-up study 2001. European Journal of Endocrinology 2002. 625–633. (10.1530/eje.0.1470625) - DOI - PubMed
-
- Stahnke N, Keller E, Landy H. & Serono Study Group. Favorable final height outcome in girls with Ullrich-Turner syndrome treated with low-dose growth hormone together with oxandrolone despite starting treatment after 10 years of age. Journal of Pediatric Endocrinology and Metabolism 2002. 129–138. (10.1515/jpem.2002.15.2.129) - DOI - PubMed
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