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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Clinical ginecologic endocrinology and infertility. J Am Coll Surg ; Rev Colomb Obstet Ginecol ; Curr Opin Obstet Gynecol ; Simon A, Chang W. N Engl J Med ; Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. Please enter User Name Password Error: Am J Obstet Gynecol ; Vaginoplasty ajenorrea intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis.

Deficiencia de alfa-hidroxilasa con cariotipo XY: Es el grupo menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados.

síndromes de galactorrea-amenorrea – English Translation – Word Magic Spanish-English Dictionary

Sign in via OpenAthens. A novel mutation of the human luteinizing hormone receptor in 46 XX sisters. Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Se puede clasificar en 3 subgrupos:. Pediatr Clin North Am ; Occurrence of myeloproliferative disorder in patients with Noonan syndrome. J and Angelman syndromes. About MyAccess 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.


Medline and Ovid databases were searched for papers published in English using the following keywords: J Endocrinol Metab ; Causas de amenorrea secundaria. El ciclo menstrual humano es susceptible a las influencias y estresantes ambientales.

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Use this site remotely Bookmark your favorite content Track your self-assessment progress and more! The genetic and galzctorrea heterogeneity of gonadotropin-releasing hormone deficiency in the human.

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Phenotypic Female External Genitalia. Impact of growth hormone supplementation on adult height in turner syndrome: Se puede clasificar en 3 subgrupos: Otherwise it is hidden from view. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH.

View Table Favorite Table Download. How to cite this article. Deficiencia de 17,20 desmolasa: Table Graphic Jump Location Cuadro Universidad de Antioquia, Colombia: Search within a content type, and even narrow to one or more resources.


Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and The neonatal presentation of Prader-Willi syndrome revisited. Pathophysiology, genetics, and treatment of hyperandrogenism. Hay C, Wu F. Es el segundo en frecuencia. Clinical and laboratory evaluation of patients with primary amenorrhea.

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: You can also find results for a single author or contributor. Pop-up div Successfully Displayed This div only appears when the trigger link is hovered over.

Etiology, diagnosis, and treatment of primary amenorrhea. Ausencia del piso de la silla turca con encefalocele anterior.

Davajan V, Kletzky OA. Genetics and hypogonadotrophic hypogonadism.