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piebaldism - decreased pigment in skin caused by disorder of pigment cells Definition for piebaldism Piebaldism is a rare autosomal dominant disorder of melanocyte development. Common characteristics include a congenital white forelock, scattered scattered normal pigmented and hyperpigmented macules and a triangular shaped depigmented patch on the forehead. Although piebaldism can be classed as partial albinism the vision problems associated with albinism are not usually present as eye pigmentation is normal. some common symptoms decreased or absent skin pigment white forelock some related diagnoses 1 - 7 of 46 diagnoses atopic dermatitis tinea versicolor pityriasis alba fungal infections skin seborrheic dermatitis drugs and toxins psoriasis   more do i have 'piebaldism'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'piebaldism' NO RESULTS piebaldism and diagnostic tests therapeutic procedures for 'piebaldism'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for piebaldism: therapeutic procedure search results for 'piebaldism' 1 - 5 of 6 therapeutic procedures rankings are computer generated. please consult your health care provider. Sun protection piebaldism and Sun protection split skin grafting piebaldism and split skin grafting Autologous punch grafting piebaldism and Autologous punch grafting Cosmetic Surgery, Dermabrasion piebaldism and Cosmetic Surgery, Dermabrasion Minigrafts piebaldism and Minigrafts Cosmetic Surgery piebaldism and Cosmetic Surgery for more please login, login is free (click to login) medications search results for 'piebaldism' rankings are computer generated. please consult your health care provider. web search results for piebaldism Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - piebaldism Piebaldism - Wikipedia, the free encyclopedia Although piebaldism can be classed as partial albinism the vision problems ... Retrieved from "http://en.wikipedia.org/wiki/Piebaldism" ... http://en.wikipedia.org/wiki/Piebaldism   en.wikipedia.org - summary A novel KIT mutation results in piebaldism with progressive depigmentation. Piebaldism is an autosomal dominant disorder of melanocyte development ... In general, piebaldism has been distinguished from vitiligo by the presence of ... http://www.ncbi.nlm.nih.gov/pubmed/11174389   www.ncbi.nlm.nih.gov - summary Permanent repigmentation of piebaldism by erbium:YAG laser and ... Permanent repigmentation of piebaldism by erbium:YAG laser and autologous cultured epidermis. ... METHODS: Six patients with piebaldism were enrolled in this study. ... http://www.ncbi.nlm.nih.gov/pubmed/15099368?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Piebaldism: an update. 1: Int J Dermatol. 2004 Oct;43(10):716-9. Piebaldism: an update. ... Piebaldism/diagnosis. Piebaldism/genetics* Piebaldism/pathology. Piebaldism/therapy ... http://www.ncbi.nlm.nih.gov/pubmed/15485525   www.ncbi.nlm.nih.gov - summary Human piebaldism: relationship between phenotype and site of kit gene ... Human piebaldism is a rare autosomal dominant disorder characterized by ... Piebaldism results from mutations of the kit proto-oncogene, which encodes a ... http://www.ncbi.nlm.nih.gov/pubmed/7544995   www.ncbi.nlm.nih.gov - summary The molecular genetics of albinism and piebaldism. Piebaldism is an autosomal-dominant congenital leukoderma associated with a white forelock. ... gene mutations causing OCA and piebaldism are as follows. ... http://www.ncbi.nlm.nih.gov/pubmed/8129415   www.ncbi.nlm.nih.gov - summary Piebaldism with deafness: molecular evidence for an expanded syndrome. Piebaldism with deafness: molecular evidence for an expanded syndrome. Spritz RA, Beighton P. ... to KIT mutations, deafness is not typical in human piebaldism. ... http://www.ncbi.nlm.nih.gov/pubmed/9450866   www.ncbi.nlm.nih.gov - summary Deletion of the KIT and PDGFRA genes in a patient with piebaldism. We have previously shown that human piebaldism results from mutations of the KIT ... DNA of a patient with piebaldism, mental retardation, and multiple congenital ... http://www.ncbi.nlm.nih.gov/pubmed/1279971   www.ncbi.nlm.nih.gov - summary KIT(CD117) - NextBio CD117: This gene encodes the human homolog of the proto-oncogene c-kit. ... Piebaldism. E2F3 gene. Milk. Squamous cell ... Mouse Phenotypes - Piebaldism ... http://www.nextbio.com/b/home/home.nb?q=CD117   www.nextbio.com - summary SNAI2 - OMIM - Genetic disorder catalog - Genetics Home Reference OMIM: Piebaldism. OMIM: SNAI2. Reviewed: April 2006. Published: February 6, 2009. Lister Hill National Center for Biomedical Communications ... http://ghr.nlm.nih.gov/gene=snai2/show/OMIM   ghr.nlm.nih.gov - summary Medical Diseases & Conditions A-Z List 'P' on MedicineNet Index of comprehensive articles on medical diseases and conditions, p listing. ... Piebaldism (Vitiligo) Pigmentary Glaucoma (Glaucoma) ... http://www.medicinenet.com/diseases_and_conditions/alpha_p.htm   www.medicinenet.com - summary Skin Center A-Z List - P on MedicineNet Information relating to the skin includes skin diseases and ... Piebaldism. Pigmented Birthmarks. Pilonidal Cyst. Pilonidal Cysts: What Are the Risk Factors? ... http://www.medicinenet.com/script/main/alphaidx.asp?p=p_25   www.medicinenet.com - summary Introduction: Pigmentation Disorders: Merck Manual Professional Focal hypo- or depigmentation is also a feature of vitiligo (which may involve ... and genetic conditions (tuberous sclerosis, piebaldism, Waardenburg's syndrome) ... http://www.merck.com/mmpe/print/sec10/ch123/ch123a.html   www.merck.com - summary SNAI2 - snail homolog 2 (Drosophila) - Genetics Home Reference What is the official name of the SNAI2 gene? ... is missing in some cases of piebaldism, a condition characterized by a white ... http://ghr.nlm.nih.gov/gene=snai2   ghr.nlm.nih.gov - summary SNAI2 - NextBio null: This gene encodes a member of the Snail family of C2H2-type ... Piebaldism. Androstanolone. Epithelium of bronchus. Waardenburg's syndrome. Dasatinib ... http://www.nextbio.com/b/home/home.nb?id=25641&type=feature   www.nextbio.com - summary Table of Contents: Dermatology emedicine features up-to-date, searchable, peer-reviewed medical journals in emergency medicine, internal medicine, ... Piebaldism. Preauricular Sinuses ... http://author.emedicine.com/derm/PEDIATRIC_DISEASES.htm   author.emedicine.com - summary 2008 MeSH Tree Structures. C17 - Skin and Connective Tissue Diseases Piebaldism [C17.800.621.440.102.600] Vitiligo [C17.800.621.440.895] ... Piebaldism [C17.800.827.080.600] Cutis Laxa [C17.800.827.180] ... http://www.nlm.nih.gov/mesh/trees2008/C17.html   www.nlm.nih.gov - summary Talk:Piebaldism - Wikipedia, the free encyclopedia I assume when you refer to domestication, you're referring to piebaldism occurring in animals? ... Retrieved from "http://en.wikipedia.org/wiki/Talk:Piebaldism" ... http://en.wikipedia.org/wiki/Talk:Piebaldism   en.wikipedia.org - summary Introduction: Pigmentation Disorders: Merck Manual Professional Ear, Nose, Throat, and Dental Disorders. Endocrine and Metabolic Disorders ... and genetic conditions (tuberous sclerosis, piebaldism, Waardenburg's syndrome) ... https://www.merck.com/mmpe/sec10/ch123/ch123a.html   /www.merck.com - summary SNAI2 - References - Genetics Home Reference Cohen ME, Yin M, Paznekas WA, Schertzer M, Wood S, Jabs EW. ... Sanchez-Garcia I. Deletion of the SLUG (SNAI2) gene results in human piebaldism. Am J Med Genet. ... http://ghr.nlm.nih.gov/gene=snai2/show/References   ghr.nlm.nih.gov - summary Albinism - NextBio general term for a number of inherited defects of amino acid ... Piebaldism ... study Mouse Phenotypes - Piebaldism. mus musculus. Mouse Phenotypes ... http://www.nextbio.com/b/home/home.nb?q=albinism   www.nextbio.com - summary 2008 MeSH Tree Structures. C18 - Nutritional and Metabolic Diseases Home > Library Catalogs and Services > MeSH. MeSH Tree Structures - 2008 ... Piebaldism [C18.452.648.100.102.600] Alkaptonuria [C18.452.648.100.187] ... http://www.nlm.nih.gov/mesh/trees2008/C18.html   www.nlm.nih.gov - summary Dominant negative and loss of function mutations of the c-kit (mast ... Piebaldism is an autosomal dominant disorder of melanocyte development and is ... We have identified c-kit gene mutations in three patients with piebaldism. ... http://www.ncbi.nlm.nih.gov/pubmed/1370874   www.ncbi.nlm.nih.gov - summary Human piebald trait resulting from a dominant negative mutant allele of ... Although the molecular basis of piebaldism has been unclear, a phenotypically ... To confirm the hypothesis that piebaldism results from mutations in the human ... http://www.ncbi.nlm.nih.gov/pubmed/1376329   www.ncbi.nlm.nih.gov - summary Mutation of the KIT (mast/stem cell growth factor receptor ... Piebaldism is an autosomal dominant genetic disorder characterized by cogenital ... Piebaldism in this family thus appears to be the human homologue to dominant ... http://www.ncbi.nlm.nih.gov/pubmed/1717985   www.ncbi.nlm.nih.gov - summary Novel mutations of the KIT (mast/stem cell growth factor receptor ... Piebaldism is an autosomal dominant genetic disorder of pigmentation ... Here we describe two novel KIT mutations associated with human piebaldism. ... http://www.ncbi.nlm.nih.gov/pubmed/7687267   www.ncbi.nlm.nih.gov - summary Graft-versus-host reaction affecting lesional skin but not normal skin ... ... disease (GVHD) arising solely within an area affected by piebaldism is described. ... differences which suggest that piebaldism-affected skin is immunologically ... http://www.ncbi.nlm.nih.gov/pubmed/8745900   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juillet ... Hits Mots-clés -446 1.44% orphanet 319 1.03% vitiligo 185 0.60% brugada syndrome ... 4 0.01% pie hendido 4 0.01% piebaldism 4 0.01% piridoxina 4 0.01% plagiozephalie ... http://orphanet.orpha.net/stat/orphanet/search_200607.html   orphanet.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Janvier ... Hits Mots-clés -423 0.83% orphanet 308 0.61% ectrodattilia 307 0.60% lupus 149 ... 0.01% pibids 4 0.01% pick 4 0.01% piebaldism 4 0.01% piel laxa 4 0.01% pierre ... http://www.orpha.net/stat/orphanet/search_200701.html   www.orpha.net - summary 2008 MeSH Tree Structures. C16 - Congenital, Hereditary, and Neonatal ... Piebaldism [C16.320.565.100.102.600] Alkaptonuria [C16.320.565.100.187] ... Piebaldism [C16.320.850.080.600] Cutis Laxa [C16.320.850.180] ... http://www.nlm.nih.gov/mesh/trees2008/C16.html   www.nlm.nih.gov - summary AceView: gene:KIT, a comprehensive annotation of human, mouse and worm ... AceView offers a comprehensive annotation of human, mouse and nematode genes reconstructed by co-alignment and clustering ... lukemia, and piebaldism. ... http://www.ncbi.nlm.nih.gov/IEB/Research/Acembly/av.cgi?db=human&l=KIT   www.ncbi.nlm.nih.gov - summary KIT and mastocytosis. ... germline loss-of-function KIT mutations have been associated with piebaldism ... Piebaldism/enzymology. Piebaldism/genetics. Proto-Oncogene Proteins c-akt ... http://www.ncbi.nlm.nih.gov/pubmed/18566536?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Fevrier ... Période du résumé: Fevrier 2007 - Mots-clés. Généré le 01-Mar-2007 22:55 CET. Hits Mots-clés -2064 3.61% maladie de marfan 1002 1.75% anpe ile-de-ré 518 0.91 ... http://www.orpha.net/stat/orphanet/search_200702.html   www.orpha.net - summary A 12-bp deletion (7818del12) in the c-kit protooncogene in a large ... 1: Hum Mutat. 1995;6(4):343-5. ... (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism. Riva P, Milani N, Gandolfi P, Larizza L. ... http://www.ncbi.nlm.nih.gov/pubmed/8680409   www.ncbi.nlm.nih.gov - summary MedicineNet - Health and Medical Information Produced by Doctors Read doctor-produced health and medical information written for you to make informed ... Piebaldism. Vitiligo RSS feed. Privacy Policy. Skin & Beauty. Get ... http://www.medicinenet.com/script/main/forum.asp?articlekey=9864   www.medicinenet.com - summary MIM Morbid map The OMIM Morbid Map presents the cytogenetic map location ... Piebaldism, 172800 (3) SNAI2, SLUG, WS2D. 602150. 8q11. Pierson syndrome, 609049 (3) LAMB2, LAMS ... http://www.ncbi.nlm.nih.gov/Omim/getmorbid.cgi?start=3245   www.ncbi.nlm.nih.gov - summary en.wikipedia.org/w/index.php?title=Piebaldism&action=history http://en.wikipedia.org/w/index.php?title=Piebaldism&action=history   en.wikipedia.org - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mars 2007 ... Période du résumé: Mars 2007 - Mots-clés. Généré le 01-Apr-2007 22:46 CEST. Hits Mots-clés -1188 1.57% ectrodactilia 580 0.76% adrenoleucodistrofia 473 0.62 ... http://www.orpha.net/stat/orphanet/search_200703.html   www.orpha.net - summary en.wikipedia.org/w/index.php?title=Piebaldism&oldid=54197260 http://en.wikipedia.org/w/index.php?title=Piebaldism&oldid=54197260   en.wikipedia.org - summary KIT - NextBio null: This gene encodes the human homolog of the proto-oncogene c-kit. ... Piebaldism. E2F3 gene. Milk. Squamous cell ... Mouse Phenotypes - Piebaldism ... http://www.nextbio.com/b/home/home.nb?id=14995&type=feature   www.nextbio.com - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Septembre ... Période du résumé: Septembre 2007 - Mots-clés. Généré le 01-Oct-2007 23:33 CEST. Hits Mots-clés -730 0.54% adrenoleucodistrofia 503 0.37% dermatomiositis 370 ... http://www.orpha.net/stat/orphanet/search_200709.html   www.orpha.net - summary MIM Gene map The OMIM Gene map presents the cytogenetic map location of disease genes and ... Piebaldism (3); Mast cell leukemia (3); Mastocytosis with associatedhematologic ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l164920   www.ncbi.nlm.nih.gov - summary MIM Gene map The OMIM Gene map presents the cytogenetic map location of disease genes and ... IID, 608890 (3); Melanoma metastasis,modification of (1); Piebaldism, 172800 (3) ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l172800   www.ncbi.nlm.nih.gov - summary Vitiligo Symptoms, Causes, Pigmentation Loss Treatment and Diagnosis on ... Information relating to the skin includes skin diseases and ... Piebaldism. Vitiligo RSS feed. Privacy Policy. Women's Health. Find out what women really need. ... http://www.medicinenet.com/vitiligo/index.htm   www.medicinenet.com - summary 164920 http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164920   www.ncbi.nlm.nih.gov - summary en.wikipedia.org/w/index.php?title=Piebaldism&oldid=70381612 http://en.wikipedia.org/w/index.php?title=Piebaldism&oldid=70381612   en.wikipedia.org - summary A Utani - NextBio Sizes of the terms below reflect their relevance to your search. ... morphea NOD2 pemphigoid perichondrium piebaldism platelet-derived growth factor ... http://www.nextbio.com/b/literature/literature.nb?author=A+Utani   www.nextbio.com - summary 172800 http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172800   www.ncbi.nlm.nih.gov - summary Horizontal and vertical pigment spread into surrounding piebald ... Following the earlier description of Carnot and Deflandre in 1896, pigment ... Piebaldism/therapy* Pigmentation* Skin Transplantation* Time Factors. Vitiligo/therapy ... http://www.ncbi.nlm.nih.gov/pubmed/10385913   www.ncbi.nlm.nih.gov - summary Simplifying the delivery of melanocytes and keratinocytes for the ... Obtaining pigmentary function in autologous skin grafts is a current challenge ... reliable robust grafting strategies for patients with vitiligo and piebaldism. ... http://www.ncbi.nlm.nih.gov/pubmed/18200063?ordinalpos=51&it...   www.ncbi.nlm.nih.gov - summary show more 1  2