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.

Author: Kazile Nazragore
Country: Benin
Language: English (Spanish)
Genre: Science
Published (Last): 18 January 2018
Pages: 187
PDF File Size: 9.53 Mb
ePub File Size: 4.48 Mb
ISBN: 308-9-50425-406-6
Downloads: 74244
Price: Free* [*Free Regsitration Required]
Uploader: Mozragore

Deficiencia de hidroxilasa con cariotipo 46, XX: Genetics and hypogonadotrophic hypogonadism. Pop-up div Successfully Displayed This div only appears when the trigger link is hovered over. Etiology, diagnosis, and treatment of primary amenorrhea. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis.

Clinical and laboratory evaluation of patients with primary amenorrhea. Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: VisitadoAbr 8. Clinical Sports Medicine Collection. The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. Please enter Password Forgot Username? Clinical ginecologic endocrinology and infertility. Psychomotor development in infants with prader-willi j and associations with sleep-related breathing disorders.

  IEC 61196 1 PDF

View Table Favorite Table Download. J Am Coll Surg ; Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. Cassidy SB, Schwartz S. This information was classified to support this review by making summaries for analysis.

Universidad de Antioquia, Colombia: Vaginoplasty using deepthelialized vulvar transposition Flaps: Am J Obstet Gynecol ; Pediatr Clin North Am ; J Clin Endocrinol Metab ; J Clin Endocrinol Metab Search Advanced search allows to you precisely focus your query. Las concentraciones de testosterona son bajas. Obstet and Gynecol ; J Endocrinol Metab ; Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency.

There was a problem providing the content you requested

Simon A, Chang W. Deficiencia de alfa-hidroxilasa con cariotipo XY: Curr Opin Obstet Gynecol ; Sign in via OpenAthens. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Charcot-Marie-Tooth disease qmenorrea Noonan syndrome with giant proximal nerve hypertrophy.

Sindrome Amenorrea Galactorrea by Carlos Mijangos Patiño on Prezi

A novel mutation of the human luteinizing hormone receptor in 46 XX sisters. Galactodrea and Angelman syndromes. Causas de amenorrea secundaria. View All Subscription Options. Occurrence of myeloproliferative disorder in patients with Noonan syndrome.


All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution Galactoorrea. Please enter User Name. An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female.

Mashchak CA y col. Se puede clasificar en 3 subgrupos: Davajan V, Kletzky OA.

You can also find results for a single author or contributor. Ausencia del piso de la silla turca con encefalocele anterior. Simon, Alex, et al. Medline and Ovid databases were searched for papers published in English using the following keywords: About MyAccess If your institution subscribes to amrnorrea resource, and you don’t have a MyAccess Profile, please contact your library’s reference desk for information on how to gain access galactorrsa this resource from off-campus.