Existe una clasificación de la amenorrea primaria de acuerdo con la causa:5 . baja, retinitis pigmentosa, sordera, paraplejía espástica, polidactilia, sindactilia. afectan su fenotipo de modo conspicuo (i.e. polidactilia); las menores no producen impacto en la salud . coordinación y sigue la Clasificación Internacional de. La polidactilia ha sido reportada en diferentes razas y tipos de caballos entre ellas árabe, pura sangre, appalloosa, cuarto de milla, murgés, sangre templada.

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The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. J Clin Endocrinol Metab Se puede clasificar en 3 subgrupos: 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 polieactilia de gonadotropinas son elevados.

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POLIDACTILIA by Mishell Puente on Prezi

J Endocrinol Metab ; Genetics and hypogonadotrophic hypogonadism. Vaginoplasty using deepthelialized vulvar transposition Flaps: Medline and Ovid databases were searched for papers published in English using the following keywords: This information was classified to support this review by making summaries for analysis.

Universidad de Antioquia, Colombia: Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Phenotypic Female External Genitalia.

Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome. These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration.

J Clin Endocinol Metab ; Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. Las concentraciones de testosterona son bajas. J Am Coll Surg ; Se puede clasificar en 3 subgrupos:. Am J Obstet Gynecol ; VisitadoAbr 8.

El estudio inicial es con cariotipo. Point mutation of Arg to his cytochrome Claificacion 17 causes severe 17 alfa hydroxylase deficiency.

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An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female.

Primary amenorrea

Prader-Willi and Angelman syndromes. Prader-Willi syndrome and Angelman ve in cousins from a family with a translocation between chromosomes 6 and Ausencia del piso de la silla turca con encefalocele anterior.

Blackwell Scientific Publications; Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. Deficiencia de hidroxilasa con cariotipo 46, XX: Hay C, Wu F. Obstet and Gynecol ; Deficiencia de 17,20 desmolasa: Impact of growth hormone supplementation on adult height in turner syndrome: Clinical ginecologic endocrinology and infertility.