equinovarus, espina bífida, polidactilia postaxial, tanatofórica, costillas cortas- polidactilia, acondroplasia, según su calidad de descripción, clasificación y. De acuerdo con la clasificación existente, la polidactilia encontrada en los miembros anteriores corresponde a la forma atavística y la encontrada en los. Este caso correspondería a este tipo de polidactilia e incluso es similar fenotípicamente a los casos confirmados cromosomalmente por otros autores como.

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Medline and Ovid calsificacion were searched for papers published in English using the following keywords: This information was classified to support this review by making summaries for analysis. It is thus important that polidactilis problem is specifically diagnosed to enable a suitable therapeutic approach to be adopted for minimising the consequences of this disease.

These questions are related to menstruation and spontaneous menstrual cycles, subsequent fertility, sexuality and the possibility of coitus with satisfactory vaginal penetration.

POLIDACTILIA by Mishell Puente on Prezi

Mashchak CA y col. Es el segundo en frecuencia.

polidavtilia Se puede clasificar polidactilla 3 subgrupos:. Deficiencia de hidroxilasa con cariotipo 46, XX: Es el grupo menos frecuente, el cariotipo es masculino y poolidactilia niveles de gonadotropinas son elevados.

Deficiencia de 17,20 desmolasa: Las concentraciones de testosterona son bajas. Deficiencia de alfa-hidroxilasa con cariotipo XY: El estudio inicial es con cariotipo. El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH.


Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: Pediatr Clin North Am ; Clinical ginecologic endocrinology and infertility. Davajan V, Kletzky OA. Phenotypic Female External Genitalia. Blackwell Scientific Publications; Clinical and laboratory evaluation of patients with primary amenorrhea.

Universidad de Antioquia, Colombia: Endocrinology and Metabolism Clinics North Am ; Hay C, Wu F. Genetics and hypogonadotrophic hypogonadism. Curr Opin Obstet Gynecol ; J Clin Endocrinol Metab ; VisitadoAbr 8.

Embriologia de la mano by Daniel Limon de Anda on Prezi

The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. Etiology, diagnosis, and treatment of primary amenorrhea.

Cassidy SB, Schwartz S. Prader-Willi and Angelman syndromes. Disorders of genomic imprinting. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

N Engl J Med ; Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders. The neonatal presentation of Prader-Willi syndrome revisited.

Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons putative satiety cells in Prader-Willi syndrome: J Endocrinol Metab ; Pediatr Phys Ther ; Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and Occurrence of myeloproliferative disorder in patients with Noonan syndrome.

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy. Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.

Growth hormona treatment in Noonan syndrome: Rev Colomb Obstet Ginecol ; Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in a patient with Swyer syndrome. Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome. Pathophysiology, genetics, and treatment of hyperandrogenism.


Point mutation of Arg pollidactilia his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency. J Clin Endocrinol Metab A novel mutation of the human luteinizing hormone receptor in 46 XX sisters.

J Clin Endocinol Metab ; An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female. The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus.

Obstet and Gynecol ; Vaginoplasty using deepthelialized vulvar transposition Flaps: J Am Coll Surg ; Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Am J Obstet Gynecol ; Impact of growth hormone supplementation on adult height in turner syndrome: All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Polydactyly of Hand

Services on Demand Article. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Se puede clasificar en 3 subgrupos: Ausencia del piso de la silla turca con encefalocele anterior. Recomendaciones para el manejo de estas pacientes Polidactklia pertinentes las siguientes recomendaciones: How to cite this article.

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