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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N Engl J Med ; Blackwell Scientific Publications; Se puede clasificar en 3 subgrupos:. El estudio inicial es con cariotipo.

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. How to cite this article. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Pediatr Phys Ther ; Occurrence of myeloproliferative disorder in patients with Noonan syndrome. Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome.


Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Rev Colomb Obstet Ginecol ; Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: Hay C, Wu F.

Primary amenorrea

Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders. The neonatal presentation of Prader-Willi syndrome revisited. Disorders of genomic imprinting. These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration. Services on Demand Article.

Universidad de Antioquia, Colombia: Obstet and Gynecol ; Impact of growth hormone supplementation on adult height in turner syndrome: Vaginoplasty using deepthelialized vulvar transposition Flaps: J Clin Endocrinol Metab ; J Clin Endocinol Metab ; The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus.

Se puede clasificar en 3 subgrupos: Pathophysiology, genetics, and treatment of hyperandrogenism. J Endocrinol Metab ; 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.

Polydactyly of Hand

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. Etiology, diagnosis, and treatment of primary amenorrhea. Es el segundo en frecuencia.


Endocrinology and Metabolism Clinics North Am polidxctilia Deficiencia de hidroxilasa con cariotipo 46, XX: This information was classified to support this review by making summaries for analysis.

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

Cassidy SB, Schwartz S. Deficiencia de alfa-hidroxilasa con cariotipo XY: Davajan V, Kletzky OA. Medline and Ovid databases were searched for papers published in English using the following keywords: Ausencia del piso de la silla turca con encefalocele anterior.

Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea dw El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH.