Výsledky vyhledávání - "Disorder of sex determination"

Akademický článek

Mullerian ducts derivatives in abdominal cryptorchism in children

Autor: S. L. Kovarsky, Yu. V. Petrukhina, S. P. Blokh, A. I. Zakharov, A. A. Bebenina

Publikováno v: Андрология и генитальная хирургия, Vol 22, Iss 4, Pp 77-85 (2021)

Disorder of sex determination is a condition associated with clinical and biochemical discrepancy between genetic, gonadal, and phenotypic sex of a child requiring detailed examination for final selection of sex. Indications for sex determination can

Externí odkaz: https://doaj.org/article/4b546da8b3d641118d21c4d7ccb6bc5e

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Familial disorder of sex determination in seven individuals from three related sibships

Autor: Ahmad Khier, Nadim Jarrah, Kamel Ajlouni, Fatima N. Obeidat, Azmi Haddidi, Hatem El-Shanti

Publikováno v: Scopus-Elsevier

In humans, the sex of an individual is determined by the Y-chromosome-related SRY gene, which causes the differentiation of the undifferentiated gonads into testicular tissue. True hermaphrodites without a Y chromosome and XX males represent a sex de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd4df55dd322f5a555d4be589849dc4a
https://pubmed.ncbi.nlm.nih.gov/11131351

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Is Hypospadias Associated with Prenatal Exposure to Endocrine Disruptors? A French Collaborative Controlled Study of a Cohort of 300 Consecutive Children Without Genetic Defect

Publikováno v: European Urology
European Urology, Elsevier, 2015, 68 (6), pp.1023-1030. ⟨10.1016/j.eururo.2015.05.008⟩

International audience; BACKGROUND:Numerous studies have focused on the association between endocrine-disrupting chemicals (EDCs) and hypospadias. Phenotype variability, the absence of representative comparison groups and concomitant genetic testing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2d74ed0aaeda56542029723faa34d33
https://pubmed.ncbi.nlm.nih.gov/26320377

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Akademický článek

Is Hypospadias Associated with Prenatal Exposure to Endocrine Disruptors? A French Collaborative Controlled Study of a Cohort of 300 Consecutive Children Without Genetic Defect.

Autor: Kalfa, Nicolas^1,2 nicolaskalfa@gmail.com, Paris, Françoise^2,3, Philibert, Pascal², Orsini, Mattea⁴, Broussous, Sylvie¹, Fauconnet-Servant, Nadège², Audran, Françoise², Gaspari, Laura², Lehors, Hélène⁵, Haddad, Myriam⁵, Guys, Jean-Michel⁵, Reynaud, Rachel⁶, Alessandrini, Pierre⁷, Merrot, Thierry⁷, Wagner, Kathy⁸, Kurzenne, Jean-Yves⁹, Bastiani, Florence⁹, Bréaud, Jean⁹, Valla, Jean-Stéphane⁹, Lacombe, Gérard Morisson¹⁰

Publikováno v: European Urology. Dec2015, Vol. 68 Issue 6, p1023-1030. 8p.

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Akademický článek

Cytogenomic Investigation of Syndromic Brazilian Patients with Differences of Sexual Development.

Autor: Faria Jr., José Antonio Diniz^1,2 (AUTHOR) danielar.moraes@gmail.com, Moraes, Daniela R.² (AUTHOR) rafael.loch@hc.fm.usp.br, Kulikowski, Leslie Domenici³ (AUTHOR) lesliekulik@gmail.com, Batista, Rafael Loch² (AUTHOR) nathalialisboa.endocrino@gmail.com, Gomes, Nathalia Lisboa² (AUTHOR) minishi@usp.br, Nishi, Mirian Yumie² (AUTHOR) beremen@usp.br, Zanardo, Evelin³ (AUTHOR) evelinzanardo@yahoo.com.br, Nonaka, Carolina Kymie Vasques^4,5 (AUTHOR) carolina.nonaka@hsr.com.br, de Freitas Souza, Bruno Solano^4,5,6 (AUTHOR) bruno.solano@fiocruz.br, Mendonca, Berenice Bilharinho² (AUTHOR), Domenice, Sorahia² (AUTHOR) sorahia.d@hc.fm.usp.br

Publikováno v: Diagnostics (2075-4418). Jul2023, Vol. 13 Issue 13, p2235. 15p.

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