Literature DB >> 18420003

Disorders of sexual development.

Thomas F Kolon1.   

Abstract

In human sexual development, the female phenotype represents the default pathway. Therefore, a failure of testis determination results in the development of the female phenotype, while genetic alterations resulting in partial testicular development can give rise to a wide spectrum of masculinization. In addition to defects in peptide hormones and their receptors, timing of hormonal exposure is also critical to appropriate development. Although much work remains to be done, recent advances in our knowledge have begun to unravel the molecular basis of disorders of sexual development. Consensus statements from investigators have recommended changes in the nomenclature, and further investigations have examined the role of the female and male psyche in patients with these disorders. This review focuses on the diagnosis and management of conditions related to disorders of sexual development.

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Year:  2008        PMID: 18420003     DOI: 10.1007/s11934-008-0030-3

Source DB:  PubMed          Journal:  Curr Urol Rep        ISSN: 1527-2737            Impact factor:   3.092


  26 in total

1.  SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite.

Authors:  E Margarit; M D Coll; R Oliva; D Gómez; A Soler; F Ballesta
Journal:  Am J Med Genet       Date:  2000-01-03

Review 2.  A practical approach to intersex in the newborn period.

Authors:  Grace Hyun; Thomas F Kolon
Journal:  Urol Clin North Am       Date:  2004-08       Impact factor: 2.241

3.  A hybrid cell mapping panel for regional localization of probes to human chromosome 8.

Authors:  M J Wagner; Y Ge; M Siciliano; D E Wells
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

4.  The incidence of intersexuality in children with cryptorchidism and hypospadias: stratification based on gonadal palpability and meatal position.

Authors:  M Kaefer; D Diamond; W H Hendren; S Vemulapalli; S B Bauer; C A Peters; A Atala; A B Retik
Journal:  J Urol       Date:  1999-09       Impact factor: 7.450

5.  Persistent müllerian duct syndrome with torsion of an intra-abdominal seminoma.

Authors:  B Masereel; G Michiels
Journal:  Acta Chir Belg       Date:  1999-10       Impact factor: 1.090

Review 6.  Congenital adrenal hyperplasia due to 3beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase deficiency.

Authors:  Jacques Simard; Anne Marie Moisan; Yves Morel
Journal:  Semin Reprod Med       Date:  2002-08       Impact factor: 1.303

7.  Dysgerminoma: the role of conservative surgery.

Authors:  A C Casey; S Bhodauria; A Shapter; R Nieberg; J S Berek; R Farias-Eisner
Journal:  Gynecol Oncol       Date:  1996-12       Impact factor: 5.482

8.  Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  Nils Krone; Felix G Riepe; Joachim Grötzinger; Carl-Joachim Partsch; Wolfgang G Sippell
Journal:  J Clin Endocrinol Metab       Date:  2004-10-13       Impact factor: 5.958

9.  Profiling transcript levels for steroidogenic enzymes in fetal tissues.

Authors:  Vincenzo Pezzi; J M Mathis; William E Rainey; Bruce R Carr
Journal:  J Steroid Biochem Mol Biol       Date:  2003-11       Impact factor: 4.292

10.  The presence of intersexuality in patients with advanced hypospadias and undescended gonads.

Authors:  M Rohatgi; P S Menon; I C Verma; J K Iyengar
Journal:  J Urol       Date:  1987-02       Impact factor: 7.450

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  1 in total

1.  Quality of life evaluation in juveniles with disorders of sexual development.

Authors:  Dan Zhu; Luhong Hu; Xiaoting Wan; Honglin Li; Qian You; Liping Gao; Jiexiong Feng
Journal:  Pediatr Surg Int       Date:  2012-10-04       Impact factor: 1.827

  1 in total

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