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Tuesday, October 14, 2008
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Reifenstein syndromeDefinitionReifenstein syndrome is one of a group of diseases in which the body is unable to respond appropriately to the male sex hormones (androgens), which include testosterone. The syndrome is passed down through families (inherited) and causes underdevelopment of the male reproductive tract. Alternative NamesPartial androgen insensitivity syndrome; Incomplete male pseudohermaphroditismCausesIn this syndrome, a problem with a gene causes cells to be less responsive to male hormones called androgens. It is also called Partial Androgen Insensitivity Syndrome. As a male baby grows in the womb, male hormones (androgens) are made. As a result, male sexual organs develop. However, sometimes there is a change in the gene that helps make a protein (receptor) that tells the body how to use androgen properly. If androgen cannot be processed normally because of a defect in this protein, problems with the development of the male sex organs occur. At birth, this may result in confusion over the sex of the baby due to ambiguous genitalia. The disease is inherited in an X-linked recessive manner, which means that women are not affected but may carry the gene. Males who inherit the gene from their mothers will have the condition. There is a 50% chance that a male child of a mother with the gene will be affected. Family history is important in determining risk factors. The syndrome is estimated to affect 1 in 99,000 people. SymptomsSymptoms include:
Exams and TestsThe doctor will perform a physical exam. The male may have:
Tests may include:
TreatmentEarly and continuous testosterone treatment may improve the chance that a boy will grow up to be fertile. Support GroupsAndrogen Insensitivity Syndrome Support Group (AISSG) -- www.medhelp.org/www/ais/ Intersex Society of North America (ISNA) -- www.isna.org Outlook (Prognosis)Androgens are most important during early development in the womb. Those with Reifenstein syndrome can have a normal lifespan and be totally healthy, with the exception of infertility and possible psychological problems related to gender identity. In the most severe cases, psychological and emotional problems may occur in boys with outer female genitalia or an extremely small penis. Management of these patients is very complex. Genital surgery should be postponed until the patient can make an informed choice. Possible Complications
When to Contact a Medical ProfessionalCall your health care provider if you, your son, or a male family member has infertility or incomplete development of male external organs, despite high blood testosterone. Genetic testing and counseling is available if there is a strong suspicion that this disease is present. PreventionPrenatal testing is available. People with a family history of these conditions should consider genetic counseling. Testosterone treatment that is started early may prevent some infertility.
Review Date: 12/11/2006 Reviewed By: Brian Kirmse, MD, Mount Sinai School of Medicine, Department of Human Genetics, New York, NY. Review provided by VeriMed Healthcare Network. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited. |