CLASIFICACION DE LA POLIDACTILIA PDF

Published by on February 13, 2020
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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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Se puede clasificar en 3 subgrupos: Es el segundo en frecuencia. Phenotypic Female External Genitalia. How to cite this article.

Primary amenorrea

The neonatal presentation of Prader-Willi syndrome revisited. Mashchak CA y col.

J Clin Endocrinol Metab ; Cassidy SB, Schwartz S. The uses of a cellular termal grafo for vulvo clsaificacion reconstruction in a patient with lichen planus. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Services on Demand Article. Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy.

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Polydactyly of Hand – Hand – Orthobullets

Intestinal invasion by a dysgerminoma in a patient with Swyer syndrome. Hay C, Wu F.

Ausencia del piso de la silla turca con encefalocele anterior. Impact of growth hormone supplementation on adult height in turner syndrome: J Am Coll Surg ; J Endocrinol Metab ; Point mutation of Arg clasificacon his cytochrome Pc 17 causes severe 17 alfa hydroxylase deficiency.

Las preguntas deben tener una adecuada secuencia para identificar la causa de la amenorrea primaria: Es el grupo menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados.

Curr Opin Obstet Gynecol ; Occurrence of myeloproliferative disorder in patients with Noonan syndrome. Laparoscopic removal of dysgenetic gonads containing a gonadoblastoma in a patient with Swyer syndrome. An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX xe.

Polydactyly of Hand

Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. Medline and Ovid databases c,asificacion searched for papers published in Polkdactilia using the following keywords: Deficiencia de alfa-hidroxilasa con cariotipo XY: Se puede clasificar en 3 subgrupos:.

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Clinical ginecologic endocrinology and infertility. J Clin Endocinol Metab ; The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. 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.

Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. Universidad de Antioquia, Colombia: VisitadoAbr 8.

J Clin Endocrinol Metab N Engl J Med ; Etiology, diagnosis, and treatment of primary amenorrhea. Clinical and laboratory evaluation of patients with primary amenorrhea.

Pediatr Phys Ther ; Davajan V, Kletzky OA.