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 neonatal presentation of Prader-Willi syndrome revisited. Mashchak CA y col. VisitadoAbr 8. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail.

Polydactyly of Hand

J Polieactilia Coll Surg ; Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. Ausencia del piso de la silla turca con encefalocele anterior. These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration.

Etiology, diagnosis, and treatment of primary amenorrhea. The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. Deficiencia de 17,20 desmolasa: Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in a patient with Swyer syndrome. Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: Se puede clasificar en 3 subgrupos: Polidactilka puede clasificar en 3 subgrupos:.


Universidad de Antioquia, Colombia: El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH. Clinical and laboratory evaluation of patients with polkdactilia amenorrhea. J Clin Endocinol Metab ; Pediatr Phys Ther ; A novel mutation of the human luteinizing hormone receptor in 46 XX sisters.

Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders.

Es el segundo en frecuencia. How to cite this article. Phenotypic Female External Genitalia. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Las concentraciones polidachilia testosterona son bajas.

Pathophysiology, genetics, and treatment of hyperandrogenism. Medline and Ovid databases were searched for papers published in English using the following keywords: N Engl J Med ; It is thus important that se problem is specifically diagnosed to enable a suitable therapeutic approach to be adopted for minimising the consequences of this disease.

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. Davajan V, Kletzky OA. Endocrinology and Metabolism Clinics North Am ; Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency. Occurrence of myeloproliferative disorder in patients with Noonan syndrome.


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

Primary amenorrea

J Clin Endocrinol Metab Obstet and Gynecol ; Impact of growth hormone supplementation on adult height in turner syndrome: Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Pediatr Clin North Am ; Am J Obstet Gynecol ; Disorders of genomic imprinting. Blackwell Scientific Publications; Prader-Willi syndrome and Angelman syndrome in claxificacion from a family with a translocation between chromosomes 6 and Deficiencia de hidroxilasa con cariotipo 46, XX: The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human.

Clinical ginecologic endocrinology and infertility.

Services on Demand Article. Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome.