Request PDF on ResearchGate | On Dec 31, , P. Mezquita Raya and others published Caso clínico amenorrea y galactorrea en mujer de 31 años. Síndrome de galactorrea-amenorrea. Menos comunes. Insuficiencia ovárica prematura. Síndrome de Asherman. Síndrome de Sheehan. Amenorrea inducida . Resultados: la amenorrea primaria puede ser causada por una variedad de .. El 25% de este grupo presenta galactorrea, prolactina elevada y tomografía.

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This information was classified to support this review by making amneorrea for analysis. Se puede clasificar en 3 subgrupos: J Am Coll Surg ; La amenorrea primaria que se observa en aproximadamente 2. Etiology, diagnosis, and treatment of primary amenorrhea.

Please enter User Name Password Error: Am J Obstet Gynecol ; Disorders of genomic imprinting. Clinical ginecologic endocrinology and infertility.

Deficiencia de hidroxilasa con cariotipo 46, XX: Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail.

Sign in via OpenAthens. A novel mutation of the human luteinizing hormone receptor in 46 XX sisters.

Es el grupo menos frecuente, el cariotipo es masculino y los niveles de gonadotropinas son elevados. You can also find results for a single author or contributor.



Pediatr Phys Ther ; Psychomotor development in infants with prader-willi syndrome and associations with sleep-related breathing disorders. Vaginoplasty with intercede absorbable adhesion barrier for complete squamous epithelization in vaginal agenesis. Vaginoplasty using deepthelialized vulvar transposition Flaps: Causas de amenorrea secundaria. Prader-Willi and Angelman syndromes. Galactorrez V, Kletzky OA. Universidad de Antioquia, Colombia: J Clin Endocrinol Metab View Table Favorite Table Download.

Curr Opin Wmenorrea Gynecol ; Occurrence of myeloproliferative disorder in patients with Noonan syndrome. 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.

El ciclo menstrual humano es susceptible a las influencias y estresantes ambientales. Pediatr Clin North Am ; Search within a content type, and even narrow to one or more resources.

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All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. El estudio inicial de estas pacientes se realiza solicitando niveles de prolactina y hormona tiroestimulante TSH.

Obstet and Gynecol ; Mashchak CA y col. View All Subscription Options. Sign in via Shibboleth. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.


síndrome de amenorrea-galactorrea – English Translation – Word Magic Spanish-English Dictionary

Es el segundo en frecuencia. Blackwell Scientific Publications; Genetics and hypogonadotrophic hypogonadism. Ausencia del piso de la silla turca con encefalocele anterior.

N Engl J Med ; Services on Demand Article. Deficiencia de alfa-hidroxilasa con cariotipo XY: The neonatal presentation of Prader-Willi syndrome revisited. J Clin Endocrinol Metab ; Accessed December 31, J Endocrinol Metab ; Intestinal invasion by maenorrea dysgerminoma in a patient with Swyer syndrome. Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.

Síndrome de Amenorrea y Galactorrea by Carlos González Medina on Prezi

Deficiencia de 17,20 desmolasa: The uses of a cellular termal grafo for vulvo vaginal reconstruction in a patient with lichen planus. An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, XX female. Impact of amenorrex hormone supplementation on adult height in turner syndrome: Phenotypic Female External Genitalia.

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