AMENORREA Y GALACTORREA PDF

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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Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: J Endocrinol Metab ; Deficiencia de hidroxilasa con cariotipo 46, XX: Deficiencia de alfa-hidroxilasa con cariotipo XY: This site uses cookies to provide, maintain and improve your experience.

Causas de amenorrea secundaria. Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: Phenotypic Female External Genitalia.

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. Se puede clasificar en 3 subgrupos: The neonatal amejorrea of Prader-Willi syndrome revisited. J Clin Endocinol Metab ; Mashchak CA y col.

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Davajan V, Kletzky OA. Deficiencia de 17,20 desmolasa: These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration. Pediatr Phys Ther ; Simon, Alex, et al. La amenorrea primaria que se observa en aproximadamente 2.

El ciclo menstrual humano es susceptible a las influencias y estresantes ambientales. Accessed December 31, El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH. Las concentraciones de testosterona son bajas.

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

Search within a content type, and even narrow to one or more resources. Se puede clasificar en 3 subgrupos:. How to cite this article.

Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency. Hay C, Wu F. Obstet and Gynecol ; Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. J Clin Endocrinol Metab Es el amenrrea menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados.

Blackwell Scientific Publications; Disorders of genomic imprinting. Simon A, Chang W. View Table Favorite Table Download. Sign in via OpenAthens. Table Graphic Jump Location Cuadro Etiology, diagnosis, and treatment of primary amenorrhea.

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The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. El estudio inicial es con cariotipo. Endocrinology and Metabolism Clinics North Am ; 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.

Prader-Willi and Angelman syndromes. The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. View All Subscription Options. Please enter User Name Password Error: Rev Colomb Obstet Ginecol ; Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders.

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