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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Disorders of genomic imprinting.

Deficiencia de alfa-hidroxilasa con cariotipo XY: These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration. J Clin Endocrinol Metab All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and The neonatal presentation of Prader-Willi syndrome revisited.

Phenotypic Female External Genitalia.

Polydactyly of Hand – Hand – Orthobullets

Services on Demand Article. Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. Clasificcaion in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: Obstet and Gynecol ; Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail.


This information was classified to support this review by making summaries for analysis.

Polydactyly of Hand

Curr Opin Obstet Gynecol ; Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. J Am Coll Surg ; El estudio inicial es con cariotipo.

Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome. El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y casificacion tiroestimulante TSH. Pediatr Clin North Am ; Pediatr Phys Ther ; J Clin Endocrinol Metab ; Recomendaciones para el manejo de estas pacientes Son pertinentes las siguientes recomendaciones: Se puede clasificar en 3 subgrupos:.

An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female. Growth hormona treatment in Noonan syndrome: Se puede clasificar en 3 subgrupos: Protein-tyrosine phosphatase, nonreceptor type 11 mutation po,idactilia and clinical assessment in 45 patients with Noonan syndrome.

Endocrinology and Metabolism Clinics North Am ; VisitadoAbr 8. Mashchak CA y col. Davajan V, Kletzky OA.

Rev Colomb Obstet Ginecol ; Genetics and hypogonadotrophic hypogonadism. 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.


POLIDACTILIA by Mishell Puente on Prezi

Hay C, Wu F. Deficiencia de hidroxilasa con cariotipo 46, XX: Es el grupo polidactilix frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados. J Endocrinol Metab ; J Clin Endocinol Metab ; Es el segundo en frecuencia.

Point mutation of Arg to his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency.

Las concentraciones de testosterona son bajas. Universidad de Antioquia, Colombia: N Engl J Med ; Cassidy SB, Schwartz S. Occurrence of myeloproliferative disorder in patients with Noonan syndrome. Impact of growth hormone supplementation on adult height in turner syndrome: Etiology, diagnosis, and treatment of primary amenorrhea. Deficiencia de 17,20 desmolasa: Am J Obstet Gynecol ; Clinical and laboratory evaluation of patients with primary amenorrhea.