The literature about Turner's syndrome was reviewed
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Turner's syndrome (TS) is one of the most common chromosomal abnormalities with an estimated frequency among female live birth of 1/4000-8000.
📊
Key Findings & Data:In this article, we presented a 10 day-old girl who admitted with carpal-pedal edema, with 45, X0 karyotype.
💡
Conclusion & Impact:The literature about Turner's syndrome was reviewed
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Turner's syndrome (TS) is one of the most common chromosomal abnormalities with an estimated frequency among female live birth of 1/4000-8000. In this article, we presented a 10 day-old girl who admitted with carpal-pedal edema, with 45, X0 karyotype. The literature about Turner's syndrome was reviewed
Özet
Turner sendromu sık rastlanılan kromozom anomalilerinden biri olup, canlı doğan kız çocuklarının 1/4000-8000'inde görülmektedir. Bu makalede el-ayak sırtı ödemi nedeniyle başvuran ve 45 X0 karyotipi gösteren 10 günlük kız çocuğu sunuldu. Turner sendromu ile ilgili literatür gözden geçirildi
🔖
Cite This Article
BAŞ, E. K., SARIKABADAYI, Y. Ü., BARLIK, M., DEMİRÇUBUK, A. G., KARCIN, M., KILIÇ, B. D. (2014). The dorsum of hand-foot edema to diagnosis: Turner Syndrome. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 48 - Sayı: 2, 153–156. https://ajindex.com/articles/399611
Bondy CA. Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. J Clin Endocrinol Metab 2007; 92: 10. Chacko E, Graber E, Regelmann MO, Wallach E, Costin G, Rapaport R. Update on Turner and Noonan syndromes. Endocrinol Metab Clin North Am 2012; 41: 713-34.
Hoskovec JM, Sinacori MK, Vidaeff. A foot path to diagnosis: prenatal sonographic identification of dorsal foot edema suggests Turner syndrome. Am J Obstet Gynecol 2013. (baskıda) Vakrilova L, Dimitrova V, Sluncheva B, Jarukova N, Pramatarova T, Shishkova R, Emilova Z. Early diagnosis of Turner Syndrome in a newborn. Akush Ginekol 2010; 49: 63-7.
Chacko EM, Rapaport R. Short stature and its treatment in Turner and Noonan syndromes. Curr Opin Endocrinol Diabetes Obes 2012; 19: 40-6.
Abir R, Fisch B, Nahum R, Orvieto R, Nitke S, Ben Rafael Z. Turner's syndrome and fertility: current status and possible putative prospects. Hum Reprod Update 2001; 7: 603-10.
Carel JC, Eugster EA, Rogol A, Ghizzoni L, Palmert MR. Consensus statement on the use of gonadotropin-releasing hormone analogs in children. Pediatrics 2009; 123: 752-62.
Hausler G, Schemper M, Frisch H. Spontaneous growth inTurner syndrome: Evidence for a minor pubertal growth spurt. In: Ranke MB, Rosenfeld RG (eds). Turner syndrome: Growth promoting therapies. Elsevier Science Publishers BV,NY, 1991: 67-73.
Chiumello G, Bognetti E, Bonfanti R, et al. Glucose metabolism in Turner syndrome. In: Ranke MB, Rosenfeld RG (eds). Turner syndrome: Growth promoting therapies. Elsevier Science Publishers BV, NY, 1991: 47-9. Davenport ML. Approach to the patient with Turner syndrome. J Clin Endocrinol Metab 2010; 95: 1487-95.
Donaldson MD, Gault EJ, Tan KW, Dunger DB. Optimising management in Turner syndrome: from infancy to adult transfer. Arch Dis Child 2006; 91: 513-20.
Karlberg J, Albertsson-Wikland K, Naerae RW. The infancy- childhood-puberty (1CP) model of growth for Turner girls. In: Ranke MB, Rosenfeld RG (eds). Turner syndrome: Growth promoting therapies. Elsevier Science Publishers BV, NY, 1991: 89-94.