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         Incontinentia Pigmenti:     more detail
  1. The Official Parent's Sourcebook on Incontinentia Pigmenti: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-11-18
  2. Incontinentia pigmenti: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005
  3. Incontinentia pigmenti may not be that rare.(News): An article from: Pediatric News by Sherry Boschert, 2008-09-01
  4. Incontinentia pigmenti lesions evolve.(Skin Disorders): An article from: Family Practice News by Doug Brunk, 2007-01-15
  5. Incontinentia pigmenti: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005
  6. Incontinentia Pigmenti - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  7. Eosinophilic Cutaneous Conditions: Churg-strauss Syndrome, Hypereosinophilic Syndrome, Incontinentia Pigmenti, Eosinophilic Granuloma
  8. Incontinentia pigmenti: treatment of IP with topical tacrolimus.(Case study): An article from: Journal of Drugs in Dermatology by Chad J. Jessup, Shane C. Morgan, et all 2009-10-01
  9. Delayed Onychodystrophy of Incontinentia pigmenti: an Evidence-based review of Epidemiology, diagnosis and management.(ORIGINAL ARTICLES)(Clinical report): ... from: Journal of Drugs in Dermatology by Sae-Ryoon Chun, Rashid M. Rashid, 2010-04-01
  10. Incontinentia pigmenti may be staged eruption in infant girls.(Clinical Rounds): An article from: Pediatric News by Doug Brunk, 2007-02-01
  11. Look for incontinentia pigmenti signs.(Clinical Rounds): An article from: Skin & Allergy News by Doug Brunk, 2007-02-01

1. Incontinentia Pigmenti
An article about this rare genetic disorder, its stages and symptoms.
http://healthlink.mcw.edu/article/921770674.html
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Incontinentia Pigmenti
Incontinentia pigmenti (IP) is a rare, genetic disorder characterized by unusual patterns of discolored skin. The disorder is caused by excessive deposits of melanin (normal skin pigment). IP is divided into 4 stages, which frequently overlap or appear together. During the first stage, which begins between birth and 6 months of age, there is inflammation accompanied by skin redness and spiral lines of small fluid-filled blisters. The second stage gradually develops with rough, warty skin growths which appear on the arms or legs and, sometimes, on the head or trunk. These growths, which are often arranged in the same spiral or linear pattern as in the first stage, usually resolve during infancy or early childhood. The third stage begins between 3 months and 2 years of age and is characterized by discolorations appearing in unusual patterns. The fourth stage consists of diminished pigmentation or atrophy in areas of previous discoloration. In rare cases of IP, hair loss with scarring and non-dermatological symptoms such as dental problems (delayed tooth growth or decay, missing or malformed teeth), diminished vision, seizures, muscle spasms, or slight paralysis may occur. Developmental abnormalities including dwarfism or short stature, club foot, spina bifida, skull and ear deformities, cleft lip or palate, atrophy on one side of the body, abnormal development of cartilage, congenital dislocation of hip, incomplete development of one side of the spinal bones, and extra ribs or webbed fingers may occur with the disorder but are not characteristic. In a few cases of IP, extremely wooly or kinky hair and an immune system dysfunction may also appear.

2. Incontinentia Pigmenti
The authors' daughter was diagnosed with IP 6 weeks after birth. This is her story.
http://mom_2_three_ip.tripod.com/
setAdGroup('67.18.104.18'); var cm_role = "live" var cm_host = "tripod.lycos.com" var cm_taxid = "/memberembedded"
Search: Lycos Tripod Free Games Share This Page Report Abuse Edit your Site ... Next Incontinentia Pigmenti Home Contact Me Comments Links to Other IP Sites ... Anna's Milestones ALL ABOUT ANNA...
This site is dedicated to my youngest child. She was diagnosed with Incontinentia Pigmenti at 6 weeks of age. This is her story, and the story of this condition. Please read on and when you are finished... feel free to contact me for questions, advice, etc. I am hoping that this site will help other families that are trying to deal with Incontinentia Pigmenti. I will try to cover most bases dealing with symptoms and give my thoughts as well. Like I said before, I am looking forward to hearing from MANY of you out there!!!
Hello All... I have removed some pages that I feel are clogging up this website. I have noticed a dwindle of people coming from this site. So here I am... finally able to update it. Please bear with me as this site will be under construction this summer... Thanks!!! This is Anna on the day she was born. April 27, 2001. She weighed 8 pounds 9 ounces and was 21 1/2 inches long.

3. IPF France
Pr©sentation de la maladie, de lassociation et de ses actions, actualit©s et liens.
http://www.orpha.net/nestasso/IPF/

4. Incontinentia Pigmenti International Foundation
This is the official site of the incontinentia pigmenti International Foundation, a charitable foundation dedicated to research into the causes and
http://imgen.bcm.tmc.edu/IPIF/
Susanne Bross Emmerich, Executive Director 30 East 72nd St, New York, N.Y. 10021 U.S.A.
Tel: 212 452-1231 Fax: 212 452-1406 E-Mail: ipif@ipif.org Web Site: http://imgen.bcm.tmc.edu/IPIF
Foundation Links
Incontinentia Pigmenti Links
Genetics and IP
Gene Discovery Links
Letter from the Founder and Executive Director Description of Incontinentia Pigmenti What is a gene? What is important about the discovery of the gene called NEMO? ... Support Groups Participate in the
IP Natural History Survey Project Where to be tested Translate: Francais Deutsch Italiano

5. Incontinentia Pigmenti Information Page National Institute Of
incontinentia pigmenti information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. EMedicine - Incontinentia Pigmenti : Article By Celia H Chang, MD
incontinentia pigmenti incontinentia pigmenti type 2, also known as Bloch-Sulzberger syndrome, is a rare, X-linked, dominantly inherited disorder of skin
http://www.emedicine.com/neuro/topic169.htm
(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Neurology Pediatric Neurology
Incontinentia Pigmenti
Last Updated: February 8, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: Bloch-Sulzberger syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Author: Celia H Chang, MD , Assistant Professor, Department of Neurology, University of California at Davis Celia H Chang, MD, is a member of the following medical societies: American Academy of Neurology , and Child Neurology Society Editor(s): David Griesemer, MD , Chairman of Neurology, Associate Professor, Departments of Pediatrics and Neurology, Medical University of South Carolina; Francisco Talavera, PharmD, PhD , Senior Pharmacy Editor, eMedicine; Kenneth J Mack, MD, PhD , Senior Associate Consultant, Department of Child and Adolescent Neurology, Mayo Clinic; Matthew J Baker, MD

7. NINDS Forwarding Page
Informational sheet compiled by National Institute of Neurological Disorders and Stroke.
http://www.ninds.nih.gov/health_and_medical/disorders/inconpig_doc.htm
NINDS has redesigned its website and the URL for the page you were seeking has changed. The new URL for this page is /disorders/incontinentia_pigmenti/incontinentia_pigmenti.htm . Please update your bookmark to this page. You will be automatically taken to this page in 5 seconds, or you can click the link to go there now.

8. Incontinentia Pigmenti
incontinentia pigmenti is a rare, genetic disorder characterized by unusual patterns of discolored skin.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. EMedicine - Incontinentia Pigmenti : Article By Takuo Tsuji, MD
incontinentia pigmenti incontinentia pigmenti (IP), sometimes termed Bloch-Sulzberger syndrome, is an X-linked dominant single-gene disorder with
http://www.emedicine.com/derm/topic698.htm
(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Dermatology Pediatric Diseases
Incontinentia Pigmenti
Last Updated: April 5, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: IP, Bloch-Sulzberger syndrome, Bloch-Siemens syndrome, familial incontinentia pigmenti, IP2 AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography
Author: Takuo Tsuji, MD , Chairman, Professor, Department of Dermatology, Nagoya City University, Japan Editor(s): Bernice R Krafchik, MB, ChB , Head, Section of Dermatology, University of Toronto; Professor, Department of Pediatrics, Hospital for Sick Children, Canada; David F Butler, MD Robert A Schwartz, MD, MPH , Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School; Joel M Gelfand, MD, MSCE

10. Incontinentia Pigmenti - 1
incontinentia pigmenti Lower leg - 3 week old baby girl. To see representative histology, click Here. Return to Image Index page.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

11. Incontinentia Pigmenti International Foundation
Details about the organization that is dedicated to research into the causes and treatment of this genetic disease. Includes information about the disease, genetics and genes.
http://imgen.bcm.tmc.edu/ipif/
Susanne Bross Emmerich, Executive Director 30 East 72nd St, New York, N.Y. 10021 U.S.A.
Tel: 212 452-1231 Fax: 212 452-1406 E-Mail: ipif@ipif.org Web Site: http://imgen.bcm.tmc.edu/IPIF
Foundation Links
Incontinentia Pigmenti Links
Genetics and IP
Gene Discovery Links
Letter from the Founder and Executive Director Description of Incontinentia Pigmenti What is a gene? What is important about the discovery of the gene called NEMO? ... Support Groups Participate in the
IP Natural History Survey Project Where to be tested Translate: Francais Deutsch Italiano

12. Incontinentia Pigmenti - 3
incontinentia pigmenti Left upper leg - 1 week old baby girl. To see representative histology, click Here. Return to Image Index page.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

13. Incontinentia Pigmenti Information Page: National Institute Of Neurological Diso
incontinentia pigmenti information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
http://www.ninds.nih.gov/disorders/incontinentia_pigmenti/incontinentia_pigmenti
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The nation's leading supporter of biomedical research on disorders of the brain and nervous system More about Incontinentia Pigmenti
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You are here: Home Disorders Incontinentia Pigmenti NINDS Incontinentia Pigmenti Information Page
Synonym(s): Bloch-Sulzberger Syndrome Get Web page suited for printing Email this to a friend or colleague Table of Contents (click to jump to sections) What is Incontinentia Pigmenti? Is there any treatment? What is the prognosis? What research is being done? ... Organizations What is Incontinentia Pigmenti? Is there any treatment? The skin abnormalities of IP usually disappear by adolescence or adulthood without treatment. Diminished vision may be treated with corrective lenses, medication, or, in severe cases, surgery. A specialist may treat dental problems. Neurological symptoms such as seizures, muscle spasms, or mild paralysis may be controlled with medication and/or medical devices and with the advice of a neurologist. What is the prognosis?

14. EMedicine - Incontinentia Pigmenti Article By Celia H Chang, MD
incontinentia pigmenti incontinentia pigmenti type 2, also known as Bloch-Sulzberger syndrome, is a rare, X-linked, dominantly inherited disorder
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

15. Introduction: Incontinentia Pigmenti - WrongDiagnosis.com
Introduction to incontinentia pigmenti as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.
http://www.wrongdiagnosis.com/i/incontinentia_pigmenti/intro.htm
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Incontinentia Pigmenti
Next sections Basic Summary for Incontinentia Pigmenti Prevalence and Incidence of Incontinentia Pigmenti Prognosis of Incontinentia Pigmenti Causes of Incontinentia Pigmenti ... Symptoms of Incontinentia Pigmenti Next chapters: Infantile Refsum Disease Infantile Spasms Joubert Syndrome Krabbé Disease ... Feedback
Introduction: Incontinentia Pigmenti
Incontinentia Pigmenti: Skin discoloration disorder Incontinentia Pigmenti: Incontinentia pigmenti (IP) is a rare, genetic disorder characterized by unusual patterns of discolored skin. The genetic transmission is X-linked dominant. Males are more severely affected than females. The disorder is caused by excessive deposits of melanin (normal skin pigment). Researching symptoms of Incontinentia Pigmenti: Further information about the symptoms of Incontinentia Pigmenti is available including a list of symptoms of Incontinentia Pigmenti , or alternatively return to research other symptoms in the symptom center Treatments for Incontinentia Pigmenti: Various information is available about treatments available for Incontinentia Pigmenti , or research treatments for other diseases.

16. Reader's Digest - Rd.com
A general discussion about incontinentia pigmenti, with alternate names and further resources.
http://www.rd.com/common/nav/index.jhtml?articleId=8612393

17. Incontinentia Pigmenti France (IPF)
incontinentia pigmenti FRANCE Bo te Postale 8128 45081 ORLEANS CEDEX 2. Association incontinentia pigmenti France
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. Symptoms Of Incontinentia Pigmenti - WrongDiagnosis.com
Symptoms of incontinentia pigmenti including signs, symptoms, incubation period, duration, and correct diagnosis.
http://www.wrongdiagnosis.com/i/incontinentia_pigmenti/symptoms.htm
Home Symptoms Diseases Risks ... Incontinentia Pigmenti Search our medical database
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Condition Lists

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Current chapter:
Incontinentia Pigmenti
Next sections Inheritance and Genetics of Incontinentia Pigmenti Treatments for Incontinentia Pigmenti Statistics about Incontinentia Pigmenti Statistics by Country for Incontinentia Pigmenti ... Articles about Incontinentia Pigmenti Next chapters: Infantile Refsum Disease Infantile Spasms Joubert Syndrome Krabbé Disease ... Feedback
Symptoms of Incontinentia Pigmenti
General information about symptoms of Incontinentia Pigmenti: The symptom information on this page attempts to provide a list of some possible symptoms of Incontinentia Pigmenti. This symptom information has been gathered from various sources, may not be fully accurate, and may not be the full list of symptoms of Incontinentia Pigmenti. Furthermore, symptoms of Incontinentia Pigmenti may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of symptoms and whether they are indeed symptoms of Incontinentia Pigmenti. List of symptoms of Incontinentia Pigmenti: The list of symptoms mentioned in various sources for Incontinentia Pigmenti includes:

19. Incontinentia Pigmenti / Family Village Library
incontinentia pigmenti Synonym BlockSiemens-Suizerger Syndrome
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

20. Incontinentia Pigmenti
incontinentia pigmenti support groups and genetic resouces.
http://www.kumc.edu/gec/support/incontin.html
Incontinentia Pigmenti
National Incontinentia Pigmenti Foundation
30 East 72nd St. New York, N.Y. 10021 U.S.A.
Phone: 212.452.1231 Fax: 212.452.1406 E-mail: nipf@pipeline.com Web Site: http://imgen.bcm.tmc.edu/NIPF
International Incontinentia Pigmenti Research Consortium
Also See: To locate a genetic counselor or clinical geneticist: Revised March 15, 2001
Genetic Societies
Clinical Resources Labs Clinics ... Search
Genetics Education Center
Debra Collins, M.S. CGC
, Genetic Counselor, dcollins@kumc.edu
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