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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Blackwell Scientific Publications; VisitadoAbr 8. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

This information was classified to support this review by making summaries for analysis. Clinical and laboratory evaluation of patients with primary amenorrhea.

Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders. A novel mutation of the human luteinizing hormone receptor in 46 XX sisters.

Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome. Phenotypic Female External Genitalia.

Prader-Willi and Angelman syndromes. Davajan V, Kletzky OA. The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. Ausencia del piso de la silla turca con encefalocele anterior. Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in a patient with Swyer syndrome.


The neonatal presentation of Prader-Willi syndrome revisited. Pediatr Phys Ther ; Pathophysiology, genetics, and treatment of hyperandrogenism.

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a clasifivacion between chromosomes 6 and Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency. Deficiencia de 17,20 desmolasa: Vaginoplasty using deepthelialized vulvar transposition Flaps: Etiology, diagnosis, and treatment of primary amenorrhea. Clinical ginecologic endocrinology and infertility. Endocrinology and Metabolism Clinics North Am ; Universidad de Antioquia, Colombia: Services on Demand Article.

Primary amenorrea

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. Se puede clasificar en 3 subgrupos: Rev Colomb Obstet Ginecol ; Am J Obstet Gynecol ; Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: N Engl J Med ; How to cite this article.

El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH. Se puede clasificar en 3 subgrupos:.

Polydactyly of Hand

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. Disorders of genomic imprinting. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Medline and Ovid databases were searched for papers published in English using the following keywords: These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration.

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J Clin Endocrinol Metab Deficiencia de alfa-hidroxilasa con cariotipo XY: Obstet and Gynecol ; Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. Deficiencia de hidroxilasa con cariotipo 46, XX: Pediatr Clin North Am ; J Endocrinol Metab ; Mashchak CA y col. J Clin Endocrinol Metab ; Growth hormona treatment in Noonan syndrome: Es el segundo en frecuencia.

Genetics and hypogonadotrophic hypogonadism. Cassidy SB, Schwartz S. An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female. Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: