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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

41. Aarskog Syndrome - [Support Group]
This information is provided as a resource and does not constitute an endorsementfor any group. It is the responsibility of the reader to decide whether a
http://www.bchealthguide.org/kbase/shc/shc29aar.htm
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Self Help Clearinghouse
Aarskog Syndrome
This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
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. Pen pals, telephone support, information and referrals, newsletter. Parents Contact Page available for networking.
WRITE:
Aarskog Syndrome Family Support Group
c/o Shannon Caranci
62 Robin Hill Lane
Levittown, PA 19055
CALL: 215-943-7131 Shannon Caranci
VERIFIED: 4/15/2004
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.

42. Aarskog Syndrome
Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/AARSKOG SYNDROME

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our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Aarskog syndrome, (Dagfinn Aarskog, born 1928, Norwegian paediatrician) (also called faciodigitogenital syndrome), X-linked recessive syndrome with the following clinical manifestations: short stature; facial abnormalities: round face, blepharoptosis, maxillary hypoplasia, broad stubby nose, long philtrum, abnormal ear position; genital abnormalities: saddle-shaped scrotum; small hands and feet. The imaging features are: short, broad metacarpals and metatarsals, clinodactyly , fusion of phalanges, hypoplasia of terminal phalanges; short tubular bones with broad metaphyses, hypoplasia of C1 with an unfused posterior arch with variable C1/C2 subluxation, 13 pairs of ribs, delayed bone age.
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43. My Grandson Has Aarskog Syndrome
My grandson, aged four, has been diagnosed as suffering from aarskog syndrome.As very little seems to be known about it I would be very grateful if y
http://www.netdoctor.co.uk/ate/childrenshealth/206296.html
Search: All NetDoctor Diseases Medicines NetDoctor.co.uk Home News and features News News archive Newsletter Features Encyclopaedia Diseases Examinations Medicines Premium services SMS services StayQuit thediet Health centres ADHD Allergy and asthma Children's health Depression ... All health centres Discussion and support Discussion forums Support groups Services Ask the doctor Find a hospital Search Medline Test yourself Information About NetDoctor Commercial opportunities NetDoctor.com My grandson has Aarskog syndrome Question
My grandson, aged four, has been diagnosed as suffering from Aarskog syndrome. As very little seems to be known about it I would be very grateful if you can provide some information about the implications and consequences of the condition.
Thanks.
Answer
Aarskog syndrome is a rare condition - only 100 or so cases are known worldwide. It is caused by a faulty gene, or genes, carried on the X chromosome. It can cause a number of physical abnormalities but a child with the syndrome won't necessarily have every one of the characteristic features. These include short stature, wide separation of the eyes, a small nose with a broad bridge, abnormally-shaped ears, short fingers and toes, undescended testicles and inguinal (groin) hernias. There may be problems with vision including a squint, astigmatism or large corneas.
Some children will have a 'caved in' appearance to their chest and a prominent umbilicus (navel). Delayed puberty may also occur but the condition is not usually associated with intellectual impairment. There is no specific treatment for Aarskog syndrome but your grandson would be expected to have a normal lifespan and he should be able to attend mainstream school. He might need surgery at some point if, for example, he has an undescended testicle or a hernia.

44. Aarskog Syndrome - Washington DC
aarskog syndrome Washington Hospital Center is located in Washington DC.
http://www.whcenter.org/12228.cfm
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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.
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

45. Aarskog Syndrome Articles, Support Groups, And Resources
aarskog syndrome articles, support groups, and resources for patients from MedHelp International (www.medhelp.org)
http://www.medhelp.org/HealthTopics/Aarskog_Syndrome.html
[Health Topics A-Z]
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B C D ... Z
Aarskog Syndrome
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Revised: 9/7/2005

46. Detail Sourcebook Listing Title Aarskog Syndrome Family Support
Title, aarskog syndrome Family Support Group networking and sharing of ideasfor families of children and adults affected with aarskog syndrome.
http://www.medhelp.org/amshc/amshc232.htm
Detail Sourcebook Listing Title: Aarskog Syndrome Family Support Group Description: Mutual support, networking and sharing of ideas for families of children and adults affected with Aarskog syndrome. Pen pals, telephone support, information and referrals, newsletter. Parents Page available for networking. Scope: International network Founded: Address: c/o Shannon Caranci
62 Robin Hill Lane
Levittown, Pennsylvania, 19055-1411
United States Telephone: Shannon Caranci (215)943-7131 This information has been generously provided by The American Self Help Clearinghouse and hosted by Med Help International . Please send corrections/updates to admin@selfhelpgroups.org
Updated: 02/2005

47. Aarskog Syndrome - Wikipedia, The Free Encyclopedia
aarskog syndrome is an inherited disease characterized by short stature, facialabnormalities, musculoskeletal, and genital anomalies.
http://en.wikipedia.org/wiki/Aarskog_syndrome
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Aarskog syndrome
From Wikipedia, the free encyclopedia.
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
Contents
edit
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

48. Aarskog Syndrome Support Group
The aarskog syndrome Support Group (UK) is no longer in operation. The familythat was running it no longer has the time and resources to continue with the
http://website.lineone.net/~gongex/
Aarskog Syndrome Support Group The Aarskog Syndrome Support Group (U.K.) is no longer in operation. The family that was running it no longer has the time and resources to continue with the Group. We apologise for any incovenience this may cause. For more information regarding the Syndrome, we suggest searching reputable medical sites.

49. Aarskog Syndrome - Overview
aarskog syndrome. Alternative names. Hypertelorism disorder; AarskogScott syndrome.Definition. An inherited disease characterized by short stature,
http://www.humed.com/humc_ency/ency/article/001654.htm
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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.

50. Disease - Aarskog Syndrome - Hartford, Connecticut
Disease aarskog syndrome - courtesy of Saint Francis Care of Hartford, Connecticut,contemporary medicine with major clinical concentrations in heart
http://www.saintfranciscare.com/1911.cfm
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Definition: Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies. Causes And Risk: 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. Prevention: There is no guaranteed prevention. Prenatal testing may be available in cases where a relative has a known mutation. 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 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

51. Hill Health Topics A-Z - Aarskog Syndrome
aarskog syndrome. National Organization for Rare Disorders. Important It ispossible that the main title of the report aarskog syndrome is not the name you
http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord615&SE

52. Aarskog Syndrome
Definition. aarskog syndrome is an inherited disease characterized by shortstature, facial abnormalities, musculoskeletal, and genital anomalies.
http://www.stv.org/adam/encyclopedia/ency/article/001654.htm
I'm going to St. Vincent's for... Pre-Admission Testing Surgery My Baby's Delivery Patient Visitation A MRI An Ultrasound A CT Scan Nuclear Medicine A Barium Enema Pain Lab / Cath Lab Mammography Mammotome Ultrasound Guided Biopsy Diagnostic Center Disease Injury Nutrition Poison ... Prevention
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 FGDY1 found on the X chromosome.
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.

53. Aarskog Syndrome - Synonyms Of Augusta, Georgia
aarskog syndrome Synonyms - University Health Care System of Augusta, Georgia.
http://www.universityhealth.org/12836.cfm

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Aarskog Syndrome
Synonyms
Disorder Subdivisions

General Discussion

Resources
...
For a Complete Report
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

54. Aarskog Syndrome Of Augusta, Georgia
aarskog syndrome University Health Care System of Augusta, Georgia.
http://www.universityhealth.org/18191.cfm

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Self-Help Resources
Information about national and local self-help organizations and support groups.
Aarskog Syndrome
This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
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. Pen pals, telephone support, information and referrals, newsletter. Parents Contact Page available for networking.
WRITE:
Aarskog Syndrome Family Support Group c/o Shannon Caranci 62 Robin Hill Lane Levittown, PA 19055 CALL: 215-943-7131 Shannon Caranci VERIFIED: 4/15/2004 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.

55. Aarskog Syndrome - St. Joseph Mercy, Ann Arbor Michigan
aarskog syndrome St. Joseph Mercy Health System Hospitals serving Ann Arbor,SE Michigan, Washtenaw County, Livingston County, Wayne County,
http://www.sjmercyhealth.org/12169.cfm
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Aarskog Syndrome
Aarskog Syndrome Family Support Group This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
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. Pen pals, telephone support, information and referrals, newsletter. Parents Contact Page available for networking.
WRITE:
Aarskog Syndrome Family Support Group
c/o Shannon Caranci
62 Robin Hill Lane
Levittown, PA 19055
CALL: 215-943-7131 Shannon Caranci
VERIFIED: 4/15/2004
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.

56. University Of Miami School Of Medicine - Glossary - Aarskog Syndrome
aarskog syndrome See AarskogScott syndrome. Glossary content Copyright ©1996-2002 MedicineNet, Inc. All rights reserved.
http://www.med.miami.edu/glossary/art.asp?articlekey=23577

57. Intelligence And Development In Aarskog Syndrome -- Logie And Porteous 79 (4): 3
Boys aged 017 years with a diagnosis of aarskog syndrome were identified The IQ in the 21 boys with aarskog syndrome studied ranged from 68-128 and
http://adc.bmjjournals.com/cgi/content/full/79/4/359

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Vol Page [Advanced] This Article Abstract Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in ADC Online Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Logie, L. J Articles by Porteous, M. E M Related Collections Genetics Arch Dis Child 359-360 ( October )
Intelligence and development in Aarskog syndrome
Lindsay J Logie, Mary E M Porteous Human Genetics Unit, University of Edinburgh, Molecular Medicine Centre, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK
Correspondence to: Dr Porteous. email: Accepted 18 April 1998
Abstract Top
Abstract
Introduction
Patients and methods
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Discussion References AIM To test the hypothesis that overall intelligence quotient (IQ) is decreased in patients with Aarskog syndrome.

58. Intelligence And Development In Aarskog Syndrome -- Logie And Porteous 79 (4): 3
study does not support the hypothesis that aarskog syndrome is associated witha lowering of mean IQ. Keywords aarskog syndrome; intelligence; genetics
http://adc.bmjjournals.com/cgi/content/abstract/79/4/359

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Vol Page [Advanced] This Article Full Text Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in ADC Online Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Logie, L. J Articles by Porteous, M. E M Related Collections Genetics Arch Dis Child 359-360 ( October )
Intelligence and development in Aarskog syndrome
Lindsay J Logie, Mary E M Porteous Human Genetics Unit, University of Edinburgh, Molecular Medicine Centre, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK
Correspondence to: Dr Porteous. email:
Accepted 18 April 1998
AIM To test the hypothesis that overall intelligence quotient (IQ) is decreased in patients with Aarskog syndrome.

59. Aarskog Syndrome
aarskog syndrome. Faciodigitogenital syndrome. aarskog syndrome aarskog syndrome Indian Pediatrics Indian Pediatrics
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=2

60. PHP : Resource Details
We would like to hear from anyone who knows anyone with aarskog syndrome. The purpose of this group is to supply any family with aarskog syndrome with
http://www.php.com/include/agency/agency_item.php?AgencyID=373&where_keywords=

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