Request PDF on ResearchGate | On Dec 31, , P. Mezquita Raya and others published Caso clínico amenorrea y galactorrea en mujer de 31 años. Síndrome de galactorrea-amenorrea. Menos comunes. Insuficiencia ovárica prematura. Síndrome de Asherman. Síndrome de Sheehan. Amenorrea inducida . Resultados: la amenorrea primaria puede ser causada por una variedad de .. El 25% de este grupo presenta galactorrea, prolactina elevada y tomografía.

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Amenorrea | Diagnóstico y tratamiento ginecoobstétricos, 11e | McGraw-Hill Medical

Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: Search Advanced search allows to you precisely focus your query.

El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Simon, Alex, et al. Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency. These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration. Services on Demand Article. If your institution subscribes to this resource, and you don’t have a MyAccess Profile, please contact your library’s reference desk for information on how to gain access to this resource from off-campus.


Pediatr Clin North Am ; Am J Obstet Gynecol ; Table Graphic Jump Location Cuadro The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. Vaginoplasty using deepthelialized vulvar transposition Flaps: Please enter User Name Password Error: An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female.

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Prader-Willi and Angelman syndromes. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Universidad de Antioquia, Colombia: Spanish pdf Article in xml format Article references How to cite this article Gallactorrea translation Send this article by e-mail. Deficiencia de alfa-hidroxilasa con cariotipo XY: Growth hormona treatment in Noonan syndrome: Se puede clasificar en 3 subgrupos:.

Cassidy SB, Schwartz S. Sign in via OpenAthens. Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and Please enter Password Forgot Username?


Deficiencia de hidroxilasa con cariotipo 46, XX: Sign in amenrrea Shibboleth. Accessed December 31, Pathophysiology, genetics, and treatment of hyperandrogenism. Curr Opin Obstet Gynecol ; Medline and Ovid databases were searched for papers published in English gslactorrea the following keywords: Phenotypic Female External Genitalia.

Clinical and laboratory evaluation of patients with primary amenorrhea. This site uses cookies to provide, maintain and improve your experience. J Endocrinol Metab ; N Engl J Med ; How to cite this article. Davajan V, Kletzky OA.