Keywords
disgenesia gonadal
pterium colli
ginecología
pediatría
pterium colli
ginecología
pediatría
How to Cite
Bustamante B., J., Molina V., I., Cardona A., F., Orrego, A., & Botero D., V. E. (2018). Variedades clínicas de la disgenesia gonadal: (revisión de 16 casos inéditos). Revista Colombiana De Endocrinología, Diabetes &Amp; Metabolismo, -6(2), 124–133. https://doi.org/10.53853/encr.-6.2.237
Abstract
Fragmento
En el presente estudio se hace una revisión de los aspectos clínicos y citológicos de 16 casos de disgenesia gonadal estudiados en los Departamentos de Medicina Interna, Ginecología y Pediatría del Hospital Universitario San Vicente de Paúl de Medellín en los años 1967 y 1968.
References
1. Wilkins L., Grumbach, M. M., Van Wyk, J. I.: Chromosomal sex in ovarian agenesis. J. Clin. Endocrin. 14: 12-70 (1954).
2. De La Chapelle: Cytogenetical and clinical observation in female gonadal dysgenesis. Acta Endocrin. Supp 65 (1942).
3. Ferguson . Smith, M. A.: Karyotype. phenotype correlacions in gonadal dygenesis and their bearning on the pathogenesis of malformations. J. Medi gen. 2: 142 (1965).
4. Blank, C. E., Gordon, R. R., Bishop, A.: Atypical Turner Syndrome. Lancet, 2: 1450 (1960).
5. Fraccaro, M., Ikkos, D., Lndsten, J., Left R., Kaijser K.: A new type of chromosomal abnormality in gonadal dysgenesis. Lancet, 2: 11-14 (1960).
6. Grumbach, M. M., Morishima A.: Chromosomal abnormalities in gonadal dysgenesis. DNA replication of structurally abnormal X chromosomes. Relation to thyroid disease.
7. Sparkes, R. S., Motulsky, A. C.: Hashimoto's disease in Turner's syndrome with isochromosome X. Lancet, 1: 947 (1963).
8. Hoffenbergg, R., Jackson, W. P.: Gonadal dysgenesis in normal looking te males. Brit. Med. J. 1: 1281 (1957).
9. Wilkins, L., Fleischman, W.: Ovarian Agenesis: pathology, associated clinical Synptoms and bearing on theories of sex differentiation. J. Clin. Endoc. 4: 457 (1944). 10. Harrnden, D. G., Stuart, J. S. S.: The chromosomes in a case of pure gonadal dysgenesis. Brit. Med. J. 2: 1287 (1959).
11. Greemblatt, R. R., Cardona N., Higdon, L.: Gonadal dysgenesis with androgenic manifestations in a tall eunucoid female. J. Clin. Endocrin. 16: 235 (1956).
12. Giusti, G., Borghi, A., Salti, M., Bigazzi, U.: “Disgenesia Gonadica Pura", con cariotipo 44 A + xx in soralle figli di cugini, Acta Genet. Med, et gem., 15: 51 (1966).
2. De La Chapelle: Cytogenetical and clinical observation in female gonadal dysgenesis. Acta Endocrin. Supp 65 (1942).
3. Ferguson . Smith, M. A.: Karyotype. phenotype correlacions in gonadal dygenesis and their bearning on the pathogenesis of malformations. J. Medi gen. 2: 142 (1965).
4. Blank, C. E., Gordon, R. R., Bishop, A.: Atypical Turner Syndrome. Lancet, 2: 1450 (1960).
5. Fraccaro, M., Ikkos, D., Lndsten, J., Left R., Kaijser K.: A new type of chromosomal abnormality in gonadal dysgenesis. Lancet, 2: 11-14 (1960).
6. Grumbach, M. M., Morishima A.: Chromosomal abnormalities in gonadal dysgenesis. DNA replication of structurally abnormal X chromosomes. Relation to thyroid disease.
7. Sparkes, R. S., Motulsky, A. C.: Hashimoto's disease in Turner's syndrome with isochromosome X. Lancet, 1: 947 (1963).
8. Hoffenbergg, R., Jackson, W. P.: Gonadal dysgenesis in normal looking te males. Brit. Med. J. 1: 1281 (1957).
9. Wilkins, L., Fleischman, W.: Ovarian Agenesis: pathology, associated clinical Synptoms and bearing on theories of sex differentiation. J. Clin. Endoc. 4: 457 (1944). 10. Harrnden, D. G., Stuart, J. S. S.: The chromosomes in a case of pure gonadal dysgenesis. Brit. Med. J. 2: 1287 (1959).
11. Greemblatt, R. R., Cardona N., Higdon, L.: Gonadal dysgenesis with androgenic manifestations in a tall eunucoid female. J. Clin. Endocrin. 16: 235 (1956).
12. Giusti, G., Borghi, A., Salti, M., Bigazzi, U.: “Disgenesia Gonadica Pura", con cariotipo 44 A + xx in soralle figli di cugini, Acta Genet. Med, et gem., 15: 51 (1966).
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