Absence of Y chromosome microdeletions in patients with cryptorchidism and hypospadias

J Pediatr Endocrinol Metab. 2004 Feb;17(2):143-8. doi: 10.1515/jpem.2004.17.2.143.

Abstract

Microdeletions of the Y chromosome have been observed in some patients with cryptorchidism and severe defects of spermatogenesis. We investigated whether microdeletions of the Y chromosome may be present in patients with cryptorchidism and hypospadias. Peripheral blood was obtained from 20 male patients 5.8 +/- 4.1 years (range: 0.4-14 years) with cryptorchidism and hypospadias for somatic DNA analysis of Y chromosome using multiplex polymerase chain reaction. These patients had no identifiable genetic syndrome, other genitourinary malformations or an abnormal karyotype. We evaluated the presence or absence of amplification using a set of 34 different sequence-tagged sites (STS) in each patient. All patients showed normal length amplifications for each of the regions evaluated, suggesting that microdeletions of the Y chromosome are not a frequent cause of hypospadias associated with cryptorchidism.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adrenal Cortex Hormones / blood
  • Child
  • Child, Preschool
  • Chorionic Gonadotropin
  • Chromosome Deletion*
  • Chromosomes, Human, Y / genetics*
  • Cryptorchidism / genetics*
  • Databases, Genetic
  • Humans
  • Hypospadias / genetics*
  • Infant
  • Karyotyping
  • Lymphocytes / ultrastructure
  • Male
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Tagged Sites
  • Sex Differentiation / genetics
  • Stimulation, Chemical
  • Testosterone / blood

Substances

  • Adrenal Cortex Hormones
  • Chorionic Gonadotropin
  • Testosterone