The Molecular Basis of Inherited Reproductive Disorders

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

Background: \- During puberty, children begin to develop into adults. Problems with the hormones released during puberty can affect the reproductive system. Some people have low hormone levels that severely delay or prevent puberty. Others start puberty abnormally early. Other people may have a normal puberty but develop reproductive disorders later in life. Researchers want to study people with reproductive disorders to learn more about how these disorders may be inherited.

Objectives: \- To learn how reproductive system disorders may be inherited.

Eligibility: * People with one of the following problems: * Abnormally early puberty * Abnormally late or no puberty * Normal puberty with hormonal problems that develop later in life * People who have not yet had puberty but have symptoms that indicate low hormone levels.

Design: * Participants will provide a blood sample for testing. They will complete a questionnaire about their symptoms. They will also have a scratch-and-sniff test to study any problems with their ability to smell. * Participant medical records will be reviewed. Participants will also provide a family medical history. * Family members of those in the study may be invited to participate. * Treatment will not be provided as part of this study....

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1 month
Maximum Age: 120
Healthy Volunteers: f
View:

⁃ The essential inclusion criteria include:

• failure to go through a normal, age-appropriate, spontaneous puberty and low sex steroid levels in the setting of low/normal gonadotropins (due to substantial variability among patient presentations, this will be based on the clinical judgement of the Investigator), or

• abnormally early development of puberty, or

• normal puberty with subsequent development of low gonadotropin levels, or

• individuals with features indicating an increased risk of hypogonadotropic hypogonadism.

• Family members: both affected and unaffected family members are strongly encouraged to participate.

Locations
United States
Maryland
National Institutes of Health Clinical Center
RECRUITING
Bethesda
North Carolina
NIEHS Clinical Research Unit (CRU)
RECRUITING
Research Triangle Park
Contact Information
Primary
NIEHS Join A Study Recruitment Group
myniehs@nih.gov
(855) 696-4347
Backup
Natalie D Shaw, M.D.
natalie.shaw@nih.gov
(984) 287-3716
Time Frame
Start Date: 2012-04-25
Participants
Target number of participants: 850
Treatments
Central Precious Puberty
CPP subjects
Hypogonadotropic Hypogonadism
IHH, KS, GnRH Deficiency, BAM syndrome (arhinia), HA, CDP subjects
Authors
Angela Delaney Freedman, Janet E Hall
Sponsors
Collaborators: Massachusetts General Hospital
Leads: National Institute of Environmental Health Sciences (NIEHS)

This content was sourced from clinicaltrials.gov