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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Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: Disorders of genomic imprinting. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Vaginoplasty using deepthelialized vulvar transposition Flaps: Medline and Ovid databases were searched for papers published in English using the following keywords: J Clin Endocinol Metab ; View All Subscription Options.

Causas de galatorrea secundaria. Please enter Password Forgot Username?

Se puede clasificar en 3 subgrupos: Use this site remotely Bookmark your favorite content Track your self-assessment progress and more! J Clin Endocrinol Metab ; Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and Las concentraciones de testosterona son bajas. An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female.


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El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH. Protein-tyrosine phosphatase, nonreceptor type 11 mutation galactorreea and clinical assessment in 45 patients with Noonan syndrome. Table Graphic Jump Location Cuadro Pathophysiology, genetics, and treatment of hyperandrogenism.

This information was classified to support this review by making summaries for analysis. Occurrence of myeloproliferative disorder in patients with Noonan syndrome.

Sindrome Amenorrea Galactorrea by Carlos Mijangos Patiño on Prezi

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Obstet and Gynecol ; The neonatal presentation of Prader-Willi syndrome revisited. Growth hormona treatment in Noonan syndrome: It is thus important that this problem is specifically diagnosed to enable a suitable therapeutic approach to be adopted for minimising the consequences of this disease.

Es el grupo menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados. N Engl J Med ; Deficiencia de alfa-hidroxilasa con cariotipo XY: Ausencia del piso de la silla turca con encefalocele anterior.


Etiology, diagnosis, and treatment of primary amenorrhea. Prader-Willi and Angelman syndromes.

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

Clinical Sports Medicine Collection. Genetics and hypogonadotrophic hypogonadism. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in a patient with Swyer syndrome.

Sign in via OpenAthens. Hay C, Wu F. Accessed December 31, Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. Es el segundo en frecuencia.

Curr Opin Obstet Gynecol ; Pediatr Clin North Am ; Clinical ginecologic endocrinology and infertility. Universidad de Antioquia, Colombia: J Clin Endocrinol Metab Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Pediatr Phys Ther ; El ciclo menstrual humano es susceptible a las influencias y estresantes ambientales.

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