CLASIFICACION DE LA POLIDACTILIA PDF

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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Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: J Endocrinol Metab ; This information was classified to support this review by making summaries for analysis.

Deficiencia de alfa-hidroxilasa con cariotipo XY: 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. Etiology, diagnosis, and treatment of primary amenorrhea. Phenotypic Polidactlia External Genitalia.

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El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH.

Primary amenorrea

VisitadoAbr 8. Deficiencia de hidroxilasa con cariotipo 46, XX: Davajan V, Kletzky OA. The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. Am J Obstet Gynecol ; Es el segundo en frecuencia.

Es el clasifixacion menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados. Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: Se puede clasificar en 3 subgrupos: How to cite this article.

J Am Coll Surg ; Pediatr Phys Ther ; The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis.

Clinical ginecologic endocrinology and infertility. The neonatal presentation of Prader-Willi syndrome revisited.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. A novel mutation of the human luteinizing hormone receptor in 46 XX sisters.

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Polydactyly of Hand

Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome. Services on Demand Article.

Vaginoplasty using deepthelialized vulvar transposition Flaps: J Clin Endocrinol Metab Genetics and hypogonadotrophic hypogonadism. Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders.

Universidad de Antioquia, Colombia: J Clin Endocinol Metab ; El estudio inicial es con cariotipo. Mashchak CA y col. Obstet and Gynecol ;