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1.
Hum Reprod ; 20(1): 279-85, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15513976

RESUMO

BACKGROUND: Hormonally active environmental agents have recently been associated with the development of endometriosis. METHODS: We undertook a study to assess the relationship between endometriosis, an estrogen-dependent gynaecological disease, and 62 individual polychlorinated biphenyl (PCBs) congeners. We enrolled 84 eligible women aged 18-40 years undergoing laparoscopy for study, which included an interview and blood specimen (n=79; 94%). Thirty-two women had visually confirmed endometriosis at laparoscopy while 52 did not. Blood specimens were run in batches of 14 including four quality control samples for toxicological analysis. Each PCB congener was adjusted for recovery; batch-specific reagent blanks were subtracted. All PCB concentrations were log transformed and expressed in ng/g serum first as a sum and then as tertiles by purported estrogenic or anti-estrogenic activity of PCB congeners. RESULTS: Using unconditional logistic regression analysis, a significantly elevated odds ratio (OR) was observed for women in the third tertile of anti-estrogenic PCBs [OR 3.77; 95% confidence interval (CI) 1.12-12.68]. Risk remained elevated after controlling for gravidity, current cigarette smoking and serum lipids (OR 3.30; 95% CI 0.87-12.46). CONCLUSIONS: These data suggest that anti-estrogenic PCBs may be associated with the development of endometriosis.


Assuntos
Endometriose/sangue , Endometriose/etiologia , Poluentes Ambientais/sangue , Poluentes Ambientais/toxicidade , Moduladores de Receptor Estrogênico/sangue , Moduladores de Receptor Estrogênico/toxicidade , Bifenilos Policlorados/sangue , Bifenilos Policlorados/toxicidade , Adolescente , Adulto , Estudos de Coortes , Moduladores de Receptor Estrogênico/química , Feminino , Humanos , Razão de Chances , Bifenilos Policlorados/química , Fatores de Risco
2.
Am J Med Genet ; 36(4): 404-7, 1990 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-2202213

RESUMO

A short-limb skeletal dysplasia was diagnosed prenatally at 35 weeks of gestation. After birth the infant was found to have hypochondroplasia. The parents are of average stature, and the child's disorder presumably occurred as a fresh mutation. This appears to be the first reported case of hypochondroplasia diagnosed prenatally as a "non-specific skeletal dysplasia" in the absence of a family history. Evaluation after birth showed that the infant, whose parents are of normal stature, has hypochondroplasia.


Assuntos
Osteocondrodisplasias/diagnóstico , Feminino , Humanos , Recém-Nascido , Gravidez , Terceiro Trimestre da Gravidez , Diagnóstico Pré-Natal , Ultrassonografia
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