May 5, 2019 posted by

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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A novel mutation of the human luteinizing hormone receptor in 46 XX sisters.

Curr Opin Obstet Gynecol ; Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in polidzctilia patient with Swyer syndrome. Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Pediatr Phys Ther ; J Clin Endocrinol Metab Blackwell Scientific Publications; VisitadoAbr 8.

Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis.

Polydactyly of Hand

Es el grupo menos frecuente, el cariotipo es masculino oolidactilia los niveles de gonadotropinas son elevados. Deficiencia de hidroxilasa con cariotipo 46, XX: J Endocrinol Metab ; Mashchak CA y col. J Am Coll Surg ; N Engl J Med ; Genetics and hypogonadotrophic hypogonadism. Es el segundo en frecuencia.


Disorders of genomic imprinting. Pathophysiology, genetics, and treatment of hyperandrogenism.

Primary amenorrea

Clinical and laboratory evaluation of patients with primary amenorrhea. Impact of growth hormone supplementation on adult height in turner syndrome: J Clin Endocinol Metab ; Hay C, Wu F. Prader-Willi and Angelman syndromes. 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 Attribution License. Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: J Clin Endocrinol Metab ; Las concentraciones de testosterona son bajas. Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy.

Deficiencia de alfa-hidroxilasa con cariotipo XY: An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female. Pediatr Clin North Am ; The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human.

Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Phenotypic Female External Genitalia.

POLIDACTILIA by Mishell Puente on Prezi

This information was classified to support this review by making summaries for analysis. Endocrinology and Metabolism Clinics North Am ; Growth hormona treatment in Noonan syndrome: Universidad de Antioquia, Colombia: Se puede clasificar en 3 subgrupos: Rev Colomb Obstet Ginecol ; Obstet and Gynecol ; Deficiencia de 17,20 desmolasa: 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.


Clinical ginecologic endocrinology and infertility. Ausencia del piso de la silla turca con encefalocele anterior.

Vaginoplasty using deepthelialized vulvar transposition Flaps: Etiology, diagnosis, and treatment of primary amenorrhea. Services on Demand Article.

Am J Obstet Gynecol ; Davajan V, Kletzky OA. Se puede clasificar en 3 subgrupos:. Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders. Medline and Ovid databases were searched for papers published in English using the following keywords: