By Heather L. Appelbaum
Comprised solely of medical circumstances protecting irregular woman puberty and its medical administration, this concise, functional casebook will offer clinicians in reproductive endocrinology, gynecology and pediatrics with the easiest real-world innovations to correctly diagnose and deal with a number of the varieties of the situation they could come across. each one bankruptcy is a case that opens with a special scientific presentation, through an outline of the analysis, evaluate and administration options used to regard it, in addition to the case end result and scientific pearls and pitfalls. instances incorporated illustrate various explanations of irregular puberty in addition to administration suggestions, together with congenital anomalies, endocrine problems, problems with constitutional hold up, weight problems, consuming issues, ovarian melanoma and the influence of pharmacology, between others. Pragmatic and reader-friendly, Abnormal lady Puberty: A medical Casebook should be a great source for reproductive endocrinologists, gynecologists and pediatricians alike.
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Extra resources for Abnormal Female Puberty: A Clinical Casebook
Those patients who do not meet criteria for surgery can be clinically monitored with examination and repeat labs and ultrasound every 6 weeks. In contrast, patients with MAS have a somatic (postzygotic) mutation of the alpha subunit of the G3 protein that leads to continued stimulation of endocrine function. Thus, for those patients who have progressive GIPP, simple observation may not be appropriate as functional ovarian cysts may not spontaneously involute, and new cysts will invariably develop.
In: Emans SJ, Laufer MR, Goldstein DP, editors. Pediatric and adolescent gynecology. 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2005. p. 487–90. 4. Oppelt PG, Lermann J, Strick R, Dittrich R, Strissel P, Rettig I, Schulze C, Renner SP, Beckmann MW, Brucker S, Rall K, Mueller A. Malformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH). Reprod Biol Endocrinol. 2012;10(1):57. 5. Patnaik SS, Brazile B, Dandolu V, Ryan PL, Liao J. Mayer-RokitanskyKüster-Hauser (MRKH) syndrome: A historical perspective.
Environmental factors and puberty timing: expert panel research needs. Pediatrics. 2008;121:192–207. 51. Cesario SK, Hughes LA. Precocious puberty: a comprehensive review of literature. J Obstet Gynecol Neonatal Nurs. 2007;36(3):263–74. 52. Özen S, Goksen D, Darcan Ş. Agricultural pesticides and precocious puberty. Vitam Horm. 2014;94:27–40. 53. Özen S, Darcan Ş. Effects of environmental endocrine disruptors on pubertal development. J Clin Res Pediatr Endocrinol. 2011;3(1):1–6. 54. Roy JR, Chakraborty S, Chakraborty TR.