Incontinentia Pigmenti (IP) (arts28.htm) Incontinentia Pigmenti (IP) (blochsulzberger syndrome). by. Dr Helen Stewart Consultant in Clinical Genetics Churchill Hospital, Oxford, UK. How common is IP? http://www.ectodermaldysplasia.org/arts28.htm
Extractions: Churchill Hospital, Oxford, UK Incontinentia Pigmenti is a rare condition, affecting girls. Only in exceptional circumstances does it affect boys. IP affects many parts of the body. It can affect different people to different degrees. There are typically four stages that occur one after the other, though they may overlap. No specific treatment is needed for the skin changes. Stage 1 There is redness of the skin, then blistering, starting from the first few weeks of life. The blisters do not affect the face but occur in lines along the limbs and round the body. Blistering usually stops by four months of age, though blisters may recur at times when the child has a temperature. During this stage, the blisters should be kept clean and dry. Stage 2 As the blisters heal, warty areas occur on the skin of the hands and feet. In most cases these clear by six months of age. Stage 3 This is the stage that gives the condition its name. There are streaks and whorls of pigment along the limbs and round the body. These darken initially, then fade, usually by the age of 16 years.
Extractions: hypopigmentation table Home Forums Privacy Advertising ... Home On this page... Introduction The table below records disorders known to involve a lack of pigment (hypopigmentation) in hair fiber. Most of the disorders are piebald traits or subcategories of albinism. This is not necessarily a complete list of disorders involving hair hypopigmentation. There are many more hypopigmentary disorders of the skin that might also involve hair. Links to relevant web pages on the Online Mendelian Inheritance in Man (OMIM) web database are also given where possible. Where a disorder is known by more than one name, alternative names are given in the second column and the record duplicated in the first column under each respective name. Brackets around alternative disorder names indicate an indirect association, for example a subcategory of the disorder. These records are not duplicated in the first column. List of disorders involving a loss of hair color (hypopigmentation) Disorders with hypopigmentation of hair as a symptom Alternative names for the disorder Links to OMIM web pages for the disorder (where available) Acrodermatitis enteropathica Zinc deficiency Albinism III Brown oculocutaneous albinism
Extractions: hypotrichosis table Home Forums Privacy Advertising ... Home On this page... Introduction The tables below records disorders known to involve hypotrichosis. The first table lists disorders where hypotrichosis is a primary symptom. The second table lists disorders where hypotrichosis can be one of several symptoms. Typically the other symptoms are of greater concern and health or life threatening. Many of these conditions involving hypotrichosis as a secondary symptom are ectodermal dysplasias. The clinical distinction between alopecia and hypotrichosis is that alopecia involves hair growth that is later lost. Hypotrichosis is a lack of any hair growth. The distinction between alopecia and hypotrichosis is not clear cut for many disorders. Some dermatologists will disagree with my listing. You may find some disorders in both the alopecia and hypotrichosis listings. This is not necessarily a complete list of disorders involving hypotrichosis. Links to relevant web pages on the Online Mendelian Inheritance in Man (OMIM) web database are also given where possible.
:: Ez2Find :: Incontinentia Pigmenti html; National Library of Medicine Site Info - Translate - Open New Window bloch-sulzberger syndrome, the synonyms, a summary and major features. http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Incontinentia Pigmenti Web Sites Incontinentia Pigmenti [Site Info] [Translate] [Open New Window] Incontinentia Pigmenti: All About Anna [Site Info] [Translate] [Open New Window] The authors' daughter was diagnosed with IP 6 weeks after birth. This is her story. URL: http://mom_2_three_ip.tripod.com/IP/
:: Ez2Find :: B Bipolar Disorder in Children (35) Birthmarks (10) Bites and Stings (30) Blastomycosis (7) Blepharospasm (10) Blindness (94) blochsulzberger syndrome (7) Blood http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode
Birth Disorder Information Directory - BA-BL Pigmenti. blochsulzberger syndrome See Incontinentia Pigmenti. Blomstrand Syndrome (Dwarfism, Lethal Type, with Advanced Bone Age) http://www.bdid.com/defectba.htm
Extractions: HOME B-K Mole Syndrome Bader Syndrome (Odontomatosis Aortae Oesophagus Stenosis, Odontoma Dysphagia Syndrome) BADS Syndrome Baelz Syndrome (Cheilitis Glandularis) Bagatelle Cassidy Syndrome (Macrocephaly Short Limbs Deafness) Bahemuka Brown Syndrome (Spastic Paraplegia Facial Cutaneous Lesions) Baker Vinters Syndrome (Hydrocephalus Craniosynostosis Bifid Nose) Ballard Syndrome (Brachydactyly, Combined B and E Types; Pitt Williams Brachydactyly) Baller Gerold Syndrome Ballinger Wallace Syndrome (Diabetes-Deafness Syndrome, Maternally Transmitted; Diabetes Mellitus, Noninsulin-Dependent/Type II, with Deafness) Bamboo Hair Syndrome Bamforth Syndrome (Hypothyroidism, Athyroidal, with Spiky Hair and Cleft Palate)
Incontinentia Pigmenti (Bloch-Sulzberger Syndrome) Seven Case Incontinentia pigmenti (blochsulzberger syndrome) seven case reports from one family. Spallone A. St Gerardo Hospital, Department http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=DocSum
Entrez PubMed Incontinentia pigmenti (blochsulzberger syndrome). Landy SJ, Donnai D. Department of Medical Genetics, St Mary s Hospital, Manchester. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra
Incontinentia Pigmenti Previews by Thumbshots National Library of Medicine bloch-sulzberger syndrome, the synonyms, a summary and major features. Previews http://www.oobdoo.com/directory/Health/ConditionsandDiseases/GeneticDisorders/In
Extractions: National Library of Medicine - Bloch-sulzberger syndrome, the synonyms, a summary and major features. MCW Healthlink: Incontinentia Pigmenti - An article about this rare genetic disorder, its stages and symptoms. Incontinentia Pigmenti - Informational sheet compiled by National Institute of Neurological Disorders and Stroke. Vanderbilt Medical Center - An article about incotinentia pigmenti. Readers Digest Health: IP - A general discussion about incontinentia pigmenti, with alternate names and further resources. 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. Incontinentia Pigmenti: All About Anna - The authors' daughter was diagnosed with IP 6 weeks after birth. This is her story.
MUMS List Of Disorders - B Benign Essential (3); Blind (490) **; blochsulzberger syndrome (Incontinentia Pigmenti) (24) *; Bloom Syndrome (4) *; Blue Sclera (2 http://www.netnet.net/mums/mum_b.htm
Extractions: indicates there is a support group which covers that diagnosis. B1A Predominent Cells or Fetal Cells (1) BOR Syndrome (Brachio-Oto-Renal Dysplasia) (7) Baller-Gerold Syndrome (Craniosynostosis-Radial Aplasia) (2) Band Heterotropia (12) Bannayan-Riley-Ruvalcaba Syndrome (8) Bannayan-Zonana Syndrome (4) Bardet-Biedl Syndrome (Laurence-Moon) (20) * http://home.talkcity.com/OceanBlvd/iamahawkfan/bardetbeidlsyndrome.html Barrett Esophagus (2) Barth Syndrome (Cardiomyopathy, Hypotonia, Low White Count) (4) www.barthsyndrome.org Basal Cell Carcinoma Syndrome (1) * Basal Cell Nevus Syndrome (1) * Basal Encephalocele (1) Basal Ganglia Infarction (1) Bassen-Kornzweig Syndrome (Abetalipoproteinemia) (2) * Bathing Suit Nevus (4) * Batten Disease (Ceroid Lipofuscinosis) (27) * Batten-Bielschowski-Jansky Disease (2) * Beals Syndrome (Contractural Arachnodactyly) (13) Beckwith-Wiedemann Syndrome (26) * Beckwith Wiedemann Family Forum Behavior Disorder (326) Behcet's Syndrome (1) * www.behcets.cc
Abstracts 5 99 VM Voinova, PV Novikov, LZ Kazantseva The blochsulzberger syndrome in children. A clinical case of the bloch-sulzberger syndrome in a child is presented. http://www.mediasphera.aha.ru/pediatr/99/5/e5-99ref.htm
Extractions: DNA diagnosis of hereditary diseases in children of the Russian Federation: State-of-the-art and problems Based on the analysis of the activities of scientific and practical medicogenetical institutions in the Russian Federation and on the data available in the literature, the paper shows the present status of DNA diagnosis of hereditary diseases in children. The available data on DNA diagnosis in the world and in Russia are critically reviewed. A spectrum of hereditary diseases detected by DNA techniques in Russia is given. The existing problems that hamper DNA technologies to be widely introduced into pediatric care are considered.
Extractions: Incontinentia Pigmenti (IP) is a rare genetic dermatological disorder affecting the skin, hair, teeth, and central nervous system. Progressive skin changes occur in four stages, the first of which appears in early infancy or is present at birth. IP is inherited as an X-linked dominant trait. Resources
NINDS Incontinentia Pigmenti Information Page Contact us Content for this page. NINDS Incontinentia Pigmenti Information Page. Synonym(s) blochsulzberger syndrome. Reviewed 12-01-2003 http://accessible.ninds.nih.gov/health_and_medical/disorders/inconpig_doc.htm
Extractions: Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders-you are in this section ... Find People The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury Studies with patients Research literature Press release NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us NINDS Incontinentia Pigmenti Information Page
About IP Bloch and Sulzberger in 1928. blochsulzberger syndrome is another name commonly used for IP. Other names are Bloch-Siemens incontinentia http://imgen.bcm.tmc.edu/IPIF/nipfchar.htm
Extractions: Tel: 212 452-1231 Fax: 212 452-1406 E-Mail: ipif@ipif.org Web Site: http://imgen.bcm.tmc.edu/IPIF by an international consortium of investigators supported by IPIF Link to Gene News return to table of contents Incontinentia Pigmenti (IP) is a genetic disease of the skin, hair, teeth and central nervous system. The condition was named because of the way the skin looks under the microscope. It was initially described in 1906 by Garrod, but the first complete description was written by Bloch and Sulzberger in 1928. "Bloch-Sulzberger Syndrome" is another name commonly used for IP. Other names are: Bloch-Siemens incontinentia pigmenti, melanoblastosis cutis linearis, and pigmented dermatosis, Siemens-Bloch type. All these names describe the same condition which we call IP. IP has not been studied in great detail until recently, so the information about it has been both limited and confusing. This discussion covers what is currently known or suspected about the disease but is not conclusive or complete. This information was taken in part from an article by Landy and Donnai, entitled "Incontinentia pigmenti (Bloch-Sulzberger syndrome)" in the Journal of Medical Genetics, 1993, pages 53-59. Medical vocabulary often can be confusing and misleading, so we recommend that parents and patients may wish to acquire a standard medical dictionary. These are available in the reference sections of most large bookstores. In general, medical writing tends to be as inclusive as possible. Therefore, descriptions of diseases or prognoses are frequently stated as "worst-case " situations. Remember that every sign, symptom, or finding is not found in every patient. Parents and patients should be selective and should interpret the information in light of their own situation(s).
Medical Information Site With Residency Directory, Auctions, Lab Oromandibular Dystonia 60) Blindness 61) Blindness, Monocular 62) Blindness, Monocular, Transient 63) Blister 64) blochsulzberger syndrome 65) Blood Pressure http://www.residency.info/dxenc/index.php?v=2&l=B
Incontinentia Pigmenti From Linkspider UK Health Directory National Library of Medicine bloch-sulzberger syndrome, the synonyms, a summary and major features. MCW Healthlink Incontinentia http://linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Incontinen
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