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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View Table Favorite Table Download. Las concentraciones de testosterona son bajas. View All Subscription Options. Es el segundo amennorrea frecuencia. Clinical and laboratory evaluation of patients with primary amenorrhea. Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and Ausencia del piso de la silla turca con encefalocele anterior.

Simon, Alex, et al. El estudio inicial es con cariotipo.

VisitadoAbr 8. About MyAccess If galactorrae 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.

Mashchak CA y col. This site uses cookies to provide, maintain and improve your experience. Davajan V, Kletzky OA. How to cite this article. Genetics and hypogonadotrophic hypogonadism.


J Clin Endocinol Metab ; Universidad de Antioquia, Colombia: Es el grupo menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados.

Blackwell Scientific Publications; Please enter Password Forgot Username? Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: Impact of growth hormone supplementation on adult height in turner syndrome: Please enter User Name.

This information was classified to support this review by making summaries for analysis. J Endocrinol Metab ; Obstet and Gynecol ; Otherwise it is hidden from view. 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.

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These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Galachorrea License.

Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency. Clinical Sports Medicine Collection. It is thus important that this problem is specifically diagnosed to enable a suitable therapeutic approach galcatorrea be adopted for minimising the consequences of this disease.


Primary amenorrea

Table Graphic Jump Location Cuadro You can also find results for a single author or contributor. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. Causas de amenorrea secundaria. J Clin Endocrinol Metab Se puede clasificar en 3 subgrupos: Hay C, Wu F.

Deficiencia de hidroxilasa con cariotipo 46, XX: Medline and Ovid databases were searched for papers published in English using the following keywords: Occurrence of myeloproliferative disorder in patients with Noonan syndrome. Growth hormona treatment in Noonan syndrome: Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in a patient with Swyer syndrome. Deficiencia de 17,20 desmolasa: Se puede clasificar en 3 subgrupos:.

Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human.

Pathophysiology, genetics, and treatment of hyperandrogenism. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis.