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Topic: Androgen insensitivity syndrome


  
 Androgen insensitivity syndrome - Wikipedia, the free encyclopedia
Variants of Reifenstein syndrome occur with greater or less androgen sensitivity and correspondingly more or less genital masculinization.
Androgenic body hair may be sparser than unaffected relatives.
At puberty, many of the early physical changes in both sexes are androgenic (adult-type body odor, increased oiliness of skin and hair, acne, pubic hair, axillary hair, fine upper lip and sideburn hair).
http://en.wikipedia.org/wiki/Androgen_insensitivity_syndrome   (4762 words)

  
 What is AIS?
Migeon et al.: Studies of the locus for androgen receptor:localization on the human X and evidence for homology with the Tfm locus in the mouse.
This affects the responsiveness, or sensitivity, of the foetus's body tissues to androgens.
For many of our members who have not been told the truth by doctors, it is these terms that they come across in medical libraries/bookshops, when searching for information that will allow them to make sense of their situation.
http://www.medhelp.org/www/ais/21_OVERVIEW.HTM   (4250 words)

  
 Androgen insensitivity syndrome and Klinefelter's syndrome
We, and other investigators [22,23] found that many of our population were treated as medical oddities, were subjected to repeated examinations, and were displayed to medical colleagues or students or photographed without their permission.
Depending upon the degree of masculinization of the genitals, the child may be raised as a boy or a girl.
Management of the condition also is related to how much freedom the individual had in expressing feelings and behaviors.
http://www.hawaii.edu/PCSS/online_artcls/intersex/AndrogenInsensitivity.htm   (8055 words)

  
 OMIM ENTRY 300068
The designation androgen insensitivity more accurately reflects the basic pathophysiology and is clearly more satisfactory to patients and their families.
Hughes and Evans (1986) described 2 sibs with classic complete androgen insensitivity syndrome but increased androgen receptor concentrations in genital skin fibroblasts.
Kaufman, M.; Pinsky, L.; Bowin, A.; Au, M. Familial external genital ambiguity due to a transformation defect of androgen-receptor complexes that is expressed with 5-alpha-dihydrotestosterone and the synthetic androgen methyltrienolone.
http://www.dur.ac.uk/~dbl0www3/MBD/Androgen.html   (4069 words)

  
 Androgen Insensitivity Syndrome Summary - Androgen Insensitivity Syndrome Information
In 2001 the British Association of Paediatric Surgeons recommended that surgery "only be undertaken with considerable caution and following full multidisciplinary investigation and counseling of the parents." Other therapies include hormone treatments and psychological counseling, including family counseling, and these are often part of the treatment, with or without surgery.
A person with PAIS may be born with external genital structures that are not typically male or typically female, a condition called intersexuality.
Gene testing and genetic counseling are available for families with affected members.
http://www.bookrags.com/sciences/genetics/androgen-insensitivity-syndrome-gen-01.html   (1671 words)

  
 [No title]
Androgen insensitivity syndrome (AIS) is a genetic condition that affects the development of the external male genitals and reproductive organs.
After a few weeks in an XY foetus, without AIS, male genitals develop under the influence of male hormones (androgens).
partially androgen insensitive (PAIS) when the external genital appearance lies somewhere between male and female.
http://www.nhsdirect.nhs.uk/articles/article.aspx?articleID=525   (186 words)

  
 AMA (Virtual Mentor) Clinical Case
Partial androgen insensitivity, unlike complete androgen insensitivity, is an intersex condition for which no general consensus exists as to the better sex assignment.
We have learned that the goal of treatment should be to promote existence of an individual who is satisfied with his or her physical appearance and has a good quality of life.
It should be emphasized again that, even among infants with the diagnosis of partial androgen insensitivity, every child and family need to be evaluated individually.
http://www.ama-assn.org/ama/pub/category/print/15625.html   (3775 words)

  
 Androgen Insensitivity Syndrome
Normal responsiveness to androgen after birth does not prove that it was normal before birth.
Normal levels of T, DHT and LH levels after birth do not prove that the level was normal during the critical period of fetal genital masculinization.
However, the great majority of such negative searches very probably reflect a "timing" problem; in other words, the acquisition of normal testosterone synthetic capacity or normal androgen responsiveness is delayed beyond the critical periods for normal external and/or internal male genital differentiation.
http://www.geneclinics.org/profiles/androgen/details.html   (4792 words)

  
 Second Type Woman - Androgen Insensitivity Syndrome
Researchers have noted that their body shape does not deviate much from that of normal females but that they tend to be larger in all body measurements, although with a tendency to a slim body.
Due to the lack of androgen affects the girl will not suffer from acne or temporal balding, and little or no pubic hair and auxiliary body hair will develop.
Lacking the effect of these androgens, the external genitals develop along female rather than male lines.
http://transwoman.tripod.com/ais.htm   (3905 words)

  
 Androgen Insensitivity Syndrome
Also, if a girl with AIS has an aunt or older sister with the same condition, she may be able to talk to that relative about what she's thinking and feeling.
The information drSpock.com provides is for educational purposes only and is not a substitute for professional medical advice.
Girls and women with androgen insensitivity syndrome, and their families, can find terrific support and information at www.medhelp.org/www/ais.
http://www.drspock.com/article/0,1510,6229,00.html   (1047 words)

  
 ANDROGEN INSENSITIVITY SYNDROME: Contact a Family - for families with disabled children: information on rare syndromes ...
The most important part of the management of AIS is the explanation and counselling given to the parents as to what and how to tell the child.
An affected infant has no virilisation, either during fetal life or during adult life.
ANDROGEN INSENSITIVITY SYNDROME: Contact a Family - for families with disabled children: information on rare syndromes and disorders
http://www.cafamily.org.uk/Direct/a48.html   (921 words)

  
 Reifenstein Syndrome
Genetic counseling may be of benefit for patients and their families.
CLINICAL AND ENDOCRINOLOGICAL CHARACTERIZATION OF TWO SUBJECTS WITH REIFENSTEIN SYNDROME ASSOCIATED WITH QUALITATIVE ABNORMALITIES OF THE ANDROGEN RECEPTOR: H.U. Schweikert et al.; Human Res (1987: issue 25(2)).
Women who are carriers of an X-linked disorder have a 50 percent risk of transmitting the carrier condition to their daughters, and a 50 percent risk of transmitting the disease to their sons.
http://hw.healthdialog.com/kbase/nord/nord844.htm   (1347 words)

  
 Testicular Feminization Syndrome (Androgen Insensitivity Syndrome) - New Treatments, May 2, 2006
Careful inspection under daylight or a white light source may reveal a brownish-yellow hyperpigmentation of the genital skin if ACTH secretion is increased (e.g., an infant with congenital adrenal hyperplasia).
Androgen insensitivity syndrome is the most studied of the disorders of sexual differentiation testicular feminization syndrome, androgen insensitivity syndrome.
Testicular Feminization Syndrome (Androgen Insensitivity Syndrome) - New Treatments, May 2, 2006
http://www.ccspublishing.com/journals4a/testicular_feminization_syndrome.htm   (700 words)

  
 Androgen insensitivity syndrome - Genetics Home Reference
This condition is inherited in an X-linked recessive pattern.
Androgen insensitivity syndrome is a condition that affects sexual development before birth and during puberty.
You might also find information on treatment of androgen insensitivity syndrome in Educational resources and Patient support.
http://ghr.nlm.nih.gov/condition=androgeninsensitivitysyndrome   (763 words)

  
 [No title]
In a family with a baby or young child with AIS, the parents will often need psychological support from a paediatric psychologist or psychiatrist to help them come to terms with their child’s condition and to help them explain the condition to their child as they grow up.
They may be treated with androgens (testosterone and/or dihydrotestosterone, DHT).
Androgen insensitivity syndrome - Treatment : NHS Direct Online
http://www.nhsdirect.nhs.uk/articles/article.aspx?articleId=525§ionId=7311   (475 words)

  
 Androgen Insensitivity Syndrome (No Uterus or Ovaries)
The most likely is one called androgen insensitivity syndrome, in which the body is programmed to develop into a male, but something happens to prevent that from happening properly.
S. Many conditions may result in the situation you report.
In this condition, the gonads (the organs that would become either ovaries or testicles) form and produce high levels of the male hormone testosterone, which would normally trigger male development -- but the body cells are unable to respond to the male hormones.
http://health.ivillage.com/gyno/0,,4q0r,00.html   (385 words)

  
 Androgen insensitivity syndrome, complete definition - Medical Dictionary definitions of popular medical terms
Many of the girls with the syndrome have no pubic or axillary (armpit) hair.
The name "complete androgen insensitivity syndrome" is scientifically accurate and is more satisfactory to patients and their families.
They are at high risk for osteoporosis and so should take estrogen replacement therapy.
http://www.medterms.com/script/main/art.asp?articlekey=14428   (374 words)

  
 Androgen Insensitivity Syndrome (AIS)
A family history of ambiguous genitals in maternal relatives suggests partial androgen insensitivity.
Androgen Insensitivity Syndrome, or AIS, is a genetic condition, inherited (except for occasional spontaneous mutations), occurring in approximately 1 in 20,000 individuals.
Hodgins M. B., Duke E. M., Ring D.: Carrier detection in the testicular feminization syndrome: deficient 5 alpha-dihydrotestosterone binding in cultured skin fibroblasts from the mothers of patients with complete androgen insensitivity.
http://www.isna.org/book/print/715   (755 words)

  
 Androgen - Wikipedia, the free encyclopedia
Circulating levels of androgens can influence human behavior because some neurons are sensitive to steroid hormones.
Androsterone: a chemical by-product created during the breakdown of androgens, or derived from progesterone, that also exerts minor masculinising effects, but with one-seventh the intensity of testosterone.
Androgens promote the enlargement of skeletal muscle cells and probably act in a coordinated manner to enhance muscle function by acting on several cell types in skeletal muscle tissue
http://en.wikipedia.org/wiki/Androgen   (3254 words)

  
 Basic Summary for Androgen Insensitivity Syndrome - WrongDiagnosis.com
Parent types of Androgen Insensitivity Syndrome: Ovary conditions, Intersex conditions
Treatments for Androgen Insensitivity Syndrome: see treatments for Androgen Insensitivity Syndrome
Symptoms of Androgen Insensitivity Syndrome: see symptoms of Androgen Insensitivity Syndrome
http://www.wrongdiagnosis.com/a/androgen_insensitivity_syndrome/basics.htm   (261 words)

  
 Androgen insensitivity syndrome : AIS
The effects of AIS are defined by the severity of the condition.
The AIS male possesses undescended testes, which provide estrogens for development of female secondary sex characteristics, but will usually need to be surgically removed due to the cancer risk.
Androgen insensitivity syndrome (AIS) is a sex-linked mutation which causes a lack of sensitivity to androgens, the male sex hormones.
http://www.fastload.org/ai/AIS.html   (320 words)

  
 Androgen Insensitivity Syndrome (AIS)
Genetic condition that eliminates the development of androgen receptors throughout the body (can occur in degrees but we’ll refer only to complete AIS).
http://courses.washington.edu/gender/b2/sld014.htm   (23 words)

  
 Info For Health » Blog Archive » Androgen insensitivity syndrome
Different degrees of androgen resistance can result in a wide variety of outward symptoms.
If the androgen insensitivity is complete, this prevents the development of the penis and other male body parts.
Call your health care provider if you have any signs or symptoms suggestive of the syndrome.
http://info-for-health.com/a/androgen-insensitivity-syndrome   (624 words)

  
 AllRefer Health - Reifenstein Syndrome (Incomplete Male Pseudohermaphroditism, Partial Androgen Insensitivity Syndrome)
You are here : AllRefer.com > Health > Diseases and Conditions > Reifenstein Syndrome
Reifenstein 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.
Reifenstein syndrome is an inherited disorder that causes underdevelopment of the male reproductive tract and sexual dysfunction in males, which includes an inability to make sperm, undescended testicles (the testicles do not descend into the scrotum), and development of breasts.
http://health.allrefer.com/health/reifenstein-syndrome-info.html   (445 words)

  
 Complete Androgen Insensitivity Syndrome
It is for women with AIS, parents of children with the condition, and health professionals involved in counselling and treating these patients.
Complete Androgen Insensitivity Syndrome is a new information booklet, published by Dr Garry Warne, Director of Endocrinology and Diabetes at RCH.
The Complete Androgen Insensitivity Syndrome booklet is also available for download.
http://www.rch.org.au/publications/CAIS.html   (116 words)

  
 GeneReviews: Androgen Insensitivity Syndrome
GeneReviews are expert-authored, peer-reviewed, current disease descriptions that apply genetic testing to the diagnosis, management, and genetic counseling of patients and families with specific inherited conditions.
Your browser does not support HTML frames so you must view Androgen Insensitivity Syndrome in a slightly less readable form.
http://www.geneclinics.org/profiles/androgen   (46 words)

  
 Androgen Insensitivity Syndrome (AIS) Support Group - Patient UK
XX conditions: Mayer Rokitansky Kuster Hauser (MRKH) Syndrome, Mullerian dysgenesis.
Androgen Insensitivity Syndrome (AIS) causes an interruption of the foetal development of the reproductive system resulting in abnormal development of reproductive organs and sometimes genitalia.
Androgen Insensitivity Syndrome (AIS) Support Group - Patient UK Androgen Insensitivity Syndrome (AIS) Support Group
http://www.patient.co.uk/showdoc/26739699   (207 words)

  
 Androgen Insensitivity Syndrome, Partial - Synonyms of Augusta, Georgia
Partial androgen insensitivity syndrome (pais) is part of a spectrum of syndromes that also includes androgen insensitivity syndrome (AIS) and mild androgen insensitivity syndrome (mais).
In partial androgen insensitivity syndrome, the development of the external genitals will be intermediate between male and female (ambiguous genitalia).
Androgen insensitivity refers to an inability of the body to respond properly to male sex hormones (androgens) produced during pregnancy.
http://www.universityhealth.org/15060.cfm   (591 words)

  
 Androgen insensitivity syndrome - A Medical Reference Article
Androgen insensitivity syndrome - A Medical Reference Article
A resource with information on over 10,000 medical topics including: Androgen insensitivity syndrome
http://www.medicalterms.org/dwp/000433.htm   (31 words)

  
 Androgen insensitivity syndrome - References - Genetics Home Reference
These sources were used to develop the Genetics Home Reference condition summary on androgen insensitivity syndrome.
Androgen insensitivity syndrome - References - Genetics Home Reference
Emery, Alan E H; Rimoin, David L; Emery and Rimoin's principles and practice of medical genetics.; 4th ed.
http://ghr.nlm.nih.gov/condition=androgeninsensitivitysyndrome/show/References   (82 words)

  
 AIS Support Group Australia Inc.
The Androgen Insensitivity Syndrome (AIS) Support Group Australia Inc. (A0041398U) is a peer support, information and advocacy group for people affected by AIS and/or related intersex conditions, and their families.
We support members (both in Australia and overseas) that have any grade of Androgen Insensitivity Syndrome, and support any issues relevant to living with AIS.
Please Note: The AIS Support Group Australia Inc. (A0041398U) is fully independent of other AIS Support Groups.
http://home.vicnet.net.au/~aissg   (421 words)

  
 Androgen Insensitivity - [Support Group]
Provides information and support to people affected by androgen insensitivity syndrome (AIS), and related conditions, including adults with the condition, parents of AIS children, and professionals working AIS.
For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
Information and referrals, phone support, regional and national support group meetings, literature, advocacy and newsletters.
http://www.peacehealth.org/kbase/shc/shc29ani.htm   (213 words)

  
 Biology Laboratory Manual  Androgen Insensitivity Syndrome
Most likely all of these women suffer from androgen insensitivity syndrome.
In the case of people with this syndrome, everything about male development occurs normally with the exception of the cells that form the embryonic sex ducts.
This will give the signal to the cells to form male sex organs.
http://highered.mcgraw-hill.com/sites/0073031216/student_view0/exercise16/androgen_insensitivity_syndrom.html   (273 words)

  
 Androgen Insensitivity Syndrome (AIS)
Can’t respond to androgen so male internal genitalia do not develop.
Can respond to Mullerian Inhibiting Factor and Inductor Substance so female internal genitalia do not develop.
http://courses.washington.edu/gender/b2/sld016.htm   (27 words)

  
 NEJM -- Androgen-Insensitivity Syndrome as a Possible Coactivator Disease
Hughes, I. A Novel Explanation for Resistance to Androgens.
NEJM -- Androgen-Insensitivity Syndrome as a Possible Coactivator Disease
This article has been cited by other articles:
http://content.nejm.org/cgi/content/short/343/12/856   (870 words)

  
 Androgen Insensitivity Syndrome > Data
Download the Androgen Insensitivity Syndrome Project raw data (unfiltered) - individual data files as well as the entire experiment set.
People involved in the Androgen Insensitivity Syndrome project
Data from the full analysis, as visualized in the Supplemental Figures, is in the following files
http://genome-www.stanford.edu/AIS/data.shtml   (128 words)

  
 Eunuch Archive Message Boards - Androgen Insensitivity Syndrome
Here is my story: 1 in 13,000 an XY genetic male fetus is unresponsive to male hormones and develops genitals that look like a girls, except for a lack of internal reproductive organs.
My name is Desire and I would like to introduce myself.
These XY coplete Androgen Insensitivity Syndrome (AIS) infants are simply declared girls and are raised as girls,
http://www.eunuch.org/vbulletin/showthread.php?t=6401   (896 words)

  
 complete androgen insensitivity syndrome (CAIS)
Endocrine system: Androgen receptor defect associated with faulty sexual differentiation due to testicular insensitivity to androgens.
Sexual ambiguity in males due to a sexual differentiation disorder caused by testicular failure to respond to androgens.
The affected males have abdominal and inguinal testes, female external genitalia and breasts, blind vaginas, and absent uteri.
http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome242.html   (138 words)

  
 Androgen-Insensitivity Syndrome
This document includes diagnosis, a clinical description, differential diagnosis, management, genetic counselling, and molecular genetics.
The Androgen Insensitivity Syndrome Support Group (AISSG) is a UK registered charity providing information to children, parents, and adults with Androgen Insensitivity Syndrome (AIS).
Notes for physicians on androgen insensitivity syndrome (AIS, Androgen Resistance Syndrome, Testicular Feminization (TFM)).
http://omni.ac.uk/browse/mesh/D013734.html   (158 words)

  
 Testicular Feminization (Complete Androgen Insensitivity Syndrome, Male Pseudohermaphroditism)
Testicular feminization occurs in a person who is genetically male and has the external appearance of a female.
Incomplete forms may happen along with a variety of unusual genetic syndromes.
Alternate Names : Complete Androgen Insensitivity Syndrome, Male Pseudohermaphroditism
http://www.3-rx.com/testicular-feminization/default.php   (180 words)

  
 Add Url - Androgen Insensitivity Syndrome -
Care Journal : Diseases and Conditions : Androgen Insensitivity Syndrome
Submit your web site to related categories only
Pay your submission fee (a PayPal payment page will open automatically once you click Submit)
http://www.carejournal.org/add_url.php?c=313   (33 words)

  
 Androgen Insensitivity Syndrome
[Androgen Resistance Syndrome, Testicular Feminization Syndrome, Feminizing Testes Syndrome, Male Pseudo-hermaphroditism, Morris's Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), Gilbert-Dreyfus Syndrome, Lubs Syndrome]
http://www.kumc.edu/gec/support/androgen.html   (65 words)

  
 Androgen Insensitivity Syndrome
Here is a link to the discussion on Jamie Leigh Curtis&; genetic syndrome.
http://arnica.csustan.edu/td/_disc1/0000001e.htm   (26 words)

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