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         Aarskog Syndrome:     more detail
  1. Genetics & Inherited Conditions: Aarskog Syndrome-galactosemia (Salem Health)
  2. Aarskog syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Roger, MD Stevenson, 2005
  3. Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02
  4. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-08-02
  5. Anomalies and Curiosities of Medicine by George M. Gould, 2010-08-02
  6. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-06-20
  7. Anomalies and Curiosities of Medicine by George M. Gould, Walter L. Pyle, 2010-09-20
  8. Anomalies And Curiosities Of Medicine- George M. Gould, A.M., M.D. by A.M., M.D. George M. Gould, 2010-02-17

21. Aarskog Syndrome Definition - Medical Dictionary Definitions Of Popular Medical
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=23577

22. 100050 AARSKOG SYNDROME 100070 ABDOMINAL AORTIC ANEURYSM 100100
100050 aarskog syndrome 100070 ABDOMINAL AORTIC ANEURYSM 100100 ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY AND
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. Aarskog Syndrome
aarskog syndrome is an extremely rare genetic disorder marked by stunted growththat may not become
http://my.webmd.com/hw/raising_a_family/nord615.asp
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Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Aarskog Syndrome Important It is possible that the main title of the report Aarskog Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
  • AAS Faciodigitogenital Syndrome Faciogenital Dysplasia FGDY Aarskog-Scott Syndrome
Disorder Subdivisions
  • None
General Discussion Aarskog syndrome is an extremely rare genetic disorder marked by stunted growth that may not become obvious until the child is about three years of age, broad facial abnormalities, musculoskeletal and genital anomalies, and mild mental retardation. Resources MAGIC Foundation for Children's Growth 6645 W. North Avenue

24. Aarskog Syndrome
International network. Founded 1993. Mutual support, networking and sharing ofideas for families of
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Who We Are About WebMD Site Map Health Topics Symptoms ... Aarskog Syndrome Family Support Group Aarskog Syndrome Aarskog Syndrome Family Support Group International network. Founded 1993. Mutual support, networking, and sharing of ideas for families of children and adults affected with Aarskog syndrome. Phone support, pen pal club, e mails addresses, and contact pages with mailing addresses for support via correspondence. WRITE: Aarskog Syndrome Family Support Group c/o Shannon Caranci 62 Robin Hill Lane Levittown, PA 19055 CALL: 215-943-7131 Shannon Caranci E-MAIL: shannonfaith49@msn.com VERIFIED: 5/6/2005 The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information. For additional information on self-help groups, please visit the American Self-Help Group Clearinghouse web site at http://www.mentalhelp.net/selfhelp

25. ► Aarskog Syndrome
A medical encycopedia article on the topic aarskog syndrome.
http://www.umm.edu/ency/article/001654.htm
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Aarskog syndrome
Overview Symptoms Treatment Prevention Definition:
Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies.
Causes, incidence, and risk factors: Aarskog syndrome is an x-linked recessive genetic disorder. This disorder affects mainly males, although females may have a milder manifestation of some of the features. It is caused by mutations in a gene called FGDY1 found on the X chromosome.
The face
Simian crease Pectus excavatum Review Date: 2/11/2002
Reviewed By: David G. Brooks, M.D., Ph.D., Division of Medical Genetics, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

26. ► Aarskog Syndrome
A medical encycopedia article on the topic aarskog syndrome.
http://www.umm.edu/ency/article/001654trt.htm
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Aarskog syndrome
Overview Symptoms Treatment Prevention Treatment:
Orthodontic treatment may be attempted for some of the facial abnormalities. Trials of growth hormone have not been effective to treat short stature in this disorder.
Support Groups: The MAGIC Foundation for Children's Growth is a support group for Aarskog syndrome and can be found at http://www.magicfoundation.org
Expectations (prognosis): Mild degrees of mental slowness may be present, but affected children usually have good social skills. Some males may exhibit reduced fertility.
Complications: Some recent findings have included cystic changes in the brain and generalized seizures . There may be difficulty growing in the first year of life in up to one third of cases. Misaligned teeth may require orthodontic correction. An undescended testicle will require surgery.
Calling your health care provider: Call your health care provider if your child exhibits delays in growth or if you notice any of the irregularities described here. Seek genetic counseling if there is Aarskog syndrome in your family. Seek evaluation by a geneticist if your doctor thinks you or your child may have Aarskog syndrome.

27. AARSKOG SYNDROME: Contact A Family - For Families With Disabled Children: Inform
Contact a Family is a UK charity for families with disabled children. We offerinformation on specific conditions and rare disorders.
http://www.cafamily.org.uk/Direct/a03.html
printer friendly AARSKOG SYNDROME home how we can help medical information index of conditions ... how you can help Did you find this page
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yes no Aarskog syndrome: Aarskog-Scott syndrome Aarskog syndrome is a rare inherited condition described in 1970 by Dr D Aarskog and Dr C I Scott in 1971. It is a development disorder characterised by short stature with facial, genital and skeletal anomalies. The condition affects mainly males, although females may have milder features. Aarskog syndrome is associated with a wide range of features and not all features of the syndrome will be found in each individual; it affects individuals differently. It has been estimated that the syndrome affects about 1:1,000,000 births but mildly affected individuals may not have been identified so the incidence may be considerably higher. Aarskog syndrome is caused by mutations in the FGDY1 gene found on the X chromosome. Aarskog syndrome is associated with :
  • a characteristic facial appearance which may include a rounded face;
  • a 'widow's peak' hairline;

28. Aarskog Syndrome Information Diseases Database
aarskog syndrome,AarskogScott syndrome,Facial-digital-genital syndrome,Faciogenitaldysplasia,Greig syndrome,Shawl scrotum syndrome, Disease Database
http://www.diseasesdatabase.com/ddb29329.htm
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Aarskog syndrome information
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6 synonyms or equivalents were found. Aarskog syndrome
aka/or
Aarskog-Scott syndrome
aka/or
Facial-digital-genital syndrome
aka/or
Faciogenital dysplasia
aka/or
Greig syndrome
aka/or Shawl scrotum syndrome Aarskog syndrome: Definition(s) via UMLS Code translations and terms via UMLS Aarskog syndrome: specific web sites Send Aarskog syndrome to medical search engines (JavaScript enabled browsers only.) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation Valid XHTML 1.0 Served 2005-09-08 18:48:45 View metadata Last major update 2005-09-03. The medical information here is presented for education, background reading and general interest. The Diseases Database is not a diagnostic or clinical decision-making tool. Please consult your own licensed physician regarding diagnosis and treatment of any medical condition!

29. Dr. Koop - Aarskog Syndrome
aarskog syndrome is an inherited disease characterized by , facial abnormalities,musculoskeletal, and genital anomalies.
http://www.drkoop.com/ency/93/001654.html
Home Health Reference Aarskog syndrome Jul 29, 2005 Search: Dr.Koop MEDLINE Diseases Symptoms Procedures Natural Medicine ... Drug Library
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Aarskog syndrome
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Aarskog syndrome
Definition: Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies.
Causes, incidence, and risk factors: Aarskog syndrome is an x-linked recessive genetic disorder. This disorder affects mainly males, although females may have a milder manifestation of some of the features. It is caused by mutations in a gene called found on the X chromosome.
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30. Aarskog Syndrome
Links to information and resources for aarskog syndrome, a genetic disorder.
http://rarediseases.about.com/cs/aarskogsyndrome/
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Guide picks A genetic disorder marked by distinctive physical abnormalities.
Aarskog Syndrome support groups

List of support groups for Aarskog syndrome. NORD: Aarskog Syndrome
Brief definition of the disorder from the National Organization for Rare Disorders (U.S.). HealthCentral: Aarskog Syndrome
Definition of the syndrome, from adam.com. Topic Index Email to a Friend
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31. Aarskog Syndrome: Information From Answers.com
aarskog syndrome aarskog syndrome is an inherited disease characterized by shortstature, facial abnormalities, musculoskeletal, and genital.
http://www.answers.com/topic/aarskog-syndrome
showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Aarskog syndrome Wikipedia Aarskog syndrome Aarskog syndrome is an inherited disease characterized by short stature, facial abnormalities, musculoskeletal, and genital anomalies. Aarskog syndrome is an x-linked recessive genetic disorder . This disorder affects mainly males, although females may have a milder manifestation of some of the features. It is caused by mutations in a gene called found on the X chromosome
Symptoms
  • mild to moderate short stature which may not be obvious until the child is between 1 and 3 years old possible delayed sexual maturation rounded face hairline has a " widow's peak wide set eyes with droopy eyelids small nose with nostrils tipped forward underdeveloped mid-portion of the face wide groove above the upper lip, crease below the lower lip delayed eruption of teeth top portion of the ear folded over slightly small, broad hands and feet with short fingers and in-curving 5th finger short fingers and toes with mild webbing simian crease (single) in palm of hand protruding belly button inguinal hernias "shawl" scrotum , undescended testicles mild to moderate mental deficiency eyes have downward palpebral slant pectus excavatum (mildly sunken chest)
Signs and tests
X-rays will reveal skeletal abnormalities.

32. Aarskog Syndrome Medical Information
aarskog syndrome Information from Drugs.com. aarskog syndrome is an inheriteddisease characterized by short stature, facial abnormalities,
http://www.drugs.com/enc/aarskog_syndrome.html

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Aarskog syndrome
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Aarskog syndrome
Definition
Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies.
Causes Aarskog syndrome is an x-linked recessive genetic disorder. This disorder affects mainly males, although females may have a milder manifestation of some of the features. It is caused by mutations in a gene called found on the X chromosome.
Symptoms
  • mild to moderate short stature which may not be obvious until the child is between 1 and 3 years old possible delayed sexual maturation rounded face hairline has a "widow's peak" wide set eyes with droopy eyelids small nose with nostrils tipped forward underdeveloped mid-portion of the face wide groove above the upper lip, crease below the lower lip

33. Aarskog Syndrome (FGD1)
aarskog syndrome is due to mutations in the FGD1 gene, a Rho/Rac guanine exchangefactor localized to Xp11.21. Males present with short stature,
http://www.ggc.org/rnadiagnostics/aarskog-fgd1.htm

34. Aarskog Syndrome
aarskog syndrome / Library / The Family Village aarskog syndrome Who to Contact Overview Symptoms Treatment Prevention aarskog syndrome Definition An
http://www.health-nexus.com/aarskog_syndrome.htm
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Aarskog Syndrome
Aarskog Syndrome / Library / The Family Village Aarskog Syndrome Who to Contact Where to Go...The Aarskog Syndrome Parents Support Group's purpose...
AARSKOG SYNDROME Pediatric Database (PEDBASE); AARSKOG SYNDROME. DEFINITION: An x-linked recessive disorder characterized ...
Aarskog syndrome ...Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome Aarskog syndrome Synonyms Aarskog-Scott syndrome (ASS) Greig syndrome facial-digital-genital syndrome...
Aarskog Syndrome Support Group (U.K.)
AARSKOG SYNDROME
Aarskog syndrome - Overview ... Overview Symptoms Treatment Prevention Aarskog syndrome Definition: An inherited disease characterized by ... anomalies. Causes, incidence, and risk factors: Aarskog syndrome is an x-linked recessive genetic disorder. This disorder ...
Aarskog Syndrome Tips for printing Aarskog Syndrome About I.B.I.S. Home ... Faciodigitogenital Syndrome Note! Aarskog Syndrome may be confused with ... Special Resources Aarskog Syndrome A Selection of Internet ... mental handicap in Aarskog syndrome may be as high as ...

35. Aarskog Syndrome- Medco.com
aarskog syndrome is an inherited disease characterized by short stature, facialabnormalities, musculoskeletal, and genital anomalies.
http://www.medcohealth.com/medco/consumer/ehealth/ehsarticle.jsp?topicID=HE:Dise

36. Aarskog Syndrome
ThirdAid.com the world s first dedicated online patient to patient medical helpcommunity. i aarskog syndrome /i is an inherited disease characterized
http://www.thirdaid.com/conditions/Aarskog_Syndrome.htm

37. Aarskog Syndrome - Alegent Health Serving Eastern Nebraska And Southwest Iowa
aarskog syndrome courtesy of Alegent Health serving eastern Nebraska andsouthwest Iowa - Council Bluffs, Iowa - Corning, Iowa - Missouri Valley,
http://www.alegent.com/1966.cfm
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Print This Page Email to a Friend The face ... Pectus excavatum
Aarskog syndrome
Definition: Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies.
Causes, incidence, and risk factors: Aarskog syndrome is an x-linked recessive genetic disorder. This disorder affects mainly males, although females may have a milder manifestation of some of the features. It is caused by mutations in a gene called found on the X chromosome.
Symptoms:
  • mild to moderate short stature which may not be obvious until the child is between 1 and 3 years old possible delayed sexual maturation rounded face hairline has a "widow's peak" wide set eyes with droopy eyelids small nose with nostrils tipped forward underdeveloped mid-portion of the face wide groove above the upper lip, crease below the lower lip delayed eruption of teeth top portion of the ear folded over slightly small, broad hands and feet with short fingers and in-curving 5th finger short fingers and toes with mild webbing simian crease (single) in palm of hand protruding belly button inguinal hernias "shawl" scrotum , undescended testicles mild to moderate mental deficiency eyes have downward palpebral slant pectus excavatum (mildly sunken chest)

Signs and tests: X-rays will reveal skeletal abnormalities. Genetic testing may be available for mutations in the

38. Aarskog Syndrome,Faciodigitogenital Syndrome,Faciogenital
aarskog syndrome,faciodigitogenital syndrome,faciogenital dysplasia,aarskogscottsyndrome,FGDY.
http://www.icomm.ca/geneinfo/aarsk.htm

39. SupportPath.com: Aarskog Syndrome
SupportPath.com leads you to Internet resources for supportrelated informationon hundreds of health, personal, and relationship topics.
http://www.supportpath.com/sl_a/aarskog_syndrome.htm
Aarskog Syndrome
An extremely rare x-linked recessive disorder characterized by short stature, facial abnormalities (broad facial features), genital anomalies, and occasional mental retardation. Also called: Aarskog-Scott syndrome (ASS), hypertelorism disorder, facial-digital-genital syndrome, facio-genital dysplasia Other topics of interest on SupportPath.com:
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40. Aarskog Syndrome
aarskog syndrome is an extremely rare genetic disorder marked by stunted growththat may not become obvious until the child is about three years of age,
http://www.bchealthguide.org/kbase/nord/nord615.htm
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National Organization for Rare Disorders, Inc.
Aarskog Syndrome
Important
It is possible that the main title of the report Aarskog Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • AAS Faciodigitogenital Syndrome Faciogenital Dysplasia FGDY Aarskog-Scott Syndrome
Disorder Subdivisions
  • None
General Discussion
Aarskog syndrome is an extremely rare genetic disorder marked by stunted growth that may not become obvious until the child is about three years of age, broad facial abnormalities, musculoskeletal and genital anomalies, and mild mental retardation.
Resources
MAGIC Foundation for Children's Growth
6645 W. North Avenue
Oak Park, IL 60302
Tel: (708)383-0808
Fax: (708)383-0899
Tel: (800)362-4423
Email: mary@magicfoundation.org
Internet: http://www.magicfoundation.org

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