RecruitingNCT01601171

Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate

The Genetics of Neuroendocrine Reproductive Disorders and of the Cleft Lip and/or Palate


Sponsor

Centre Hospitalier Universitaire Vaudois

Enrollment

2,000 participants

Start Date

Mar 1, 2012

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to explore the genetic basis of reproductive disorders and cleft lip and/or palate.


Eligibility

Inclusion Criteria9

  • hypogonadotropic hypogonadism
  • Kallmann syndrome
  • adult-onset hypogonadotropic hypogonadism
  • hypothalamic amenorrhea
  • polycystic ovarian syndrome
  • primary gonadal failure
  • precocious puberty
  • cleft lip/palate
  • family members of the above groups

Exclusion Criteria7

  • acute illness/hospitalization
  • pituitary tumors
  • iron overload (hemochromatosis)
  • infiltrative diseases (sarcoidosis)
  • chronic alcohol abuse
  • illicit drug use
  • anabolic steroid abuse

Locations(1)

Centre Hospitalier Universitaire Vaudois (CHUV)

Lausanne, Canton of Vaud, Switzerland

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NCT01601171


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