81. Untitled Document Usher waardenburg. Mitochondrial hearing impairment (syndromic and nonsyndromic) is given separately. Alport syndrome http://www.uia.ac.be/dnalab/hhh/syndromi.html

82. Waardenburg, Syndrome : Sites Et Documents Francophones Translate this page Arborescence(s) du thesaurus MeSH contenant le mot-clé waardenburg,syndrome waardenburg's syndrome maladies et malformations http://www.chu-rouen.fr/ssf/pathol/waardenburgsyndrome.html

Waardenburg, Syndrome Menu général CISMeF Arborescence(s) Waardenburg, syndrome Waardenburg's syndrome maladies et malformations congénitales, héréditaires et néonatales Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : guide ressources Waardenburg type 1, syndrome de [Par Dr Faivre L, Pr Vekemans M. Site éditeur Orphanet mots clés : signes et symptômes Waardenburg, syndrome type(s) : guide ressources structure recherche texte association patients ... Waardenburg type 2, syndrome de - synonymes : Waardenburg type 2A, syndrome de ; Waardenburg type 2B, syndrome de [Par Dr Faivre L, Pr Vekemans M. Site éditeur Orphanet mots clés : signes et symptômes Waardenburg, syndrome type(s) : guide ressources structure recherche texte association patients ... Waardenburg type 3, syndrome de - synonyme : Klein-Waardenburg, syndrome de [Par Dr Faivre L, Pr Vekemans M.

83. Waardenburg, Syndrome : Arborescences MeSH Translate this page waardenburg, syndrome. waardenburg, syndrome C16.131.077.938 page CISMeFdu motclef Wolfram, syndrome C16.131.077.951 page CISMeF du motclef http://www.chu-rouen.fr/navimesh/naviwaardenburgsyndrome.html

Waardenburg, Syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF maladies et malformations congénitales, héréditaires et néonatales malformations malformations multiples Alagille, syndrome ... Zellweger, syndrome 27 février 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

84. Waardenburg's Syndrome Expand your medical search to other sites by only one click . For MedicalProfessionals only. waardenburg's syndrome,, Print this article, http://www.amershamhealth.com/medcyclopaedia/Volume III 1/WAARDENBURGS SYNDROME.

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Waardenburg's syndrome, (Petrus Johannes Waardenburg, 1886–1979, Dutch ophthalmologist), a form of acrocephalosyndactyly of unknown inheritance characterized by moderate acrocephaly, pointed nose, contractures and eye abnormalities. Other features include hypoplastic maxilla, asymmetry of hands, deformity of the first phalanx of the hand, absence of the first digit of the foot and bifid distal phalanges of the second and third toes. DR The Encyclopaedia of Medical Imaging Volume III:1 Welcome to Medcyclopaedia. This site is open to a public audience, still we want to know a little more about our visitors. Please tick off the boxes that match your profile. Do you live in Europe?

85. ILDS: ICD-10 - By Disorder [Waardenburg's Syndrome - Wyburn Mason Syndrome] ICD Code Disorder, E70308 waardenburg's syndrome, C880 Waldenström's macroglobulinemia,A630 Wart anogenital, B07x09 Wart common (NOS), B07x02 Wart digitate, http://www.ilds.org/icd10/bydisorder/W.html

Application to Dermatology of ICD-10 Alphabetized by Disorder starting with W: Return to Alphabetical listing... ICD Code: Disorder Waardenburg's syndrome Waldenström's macroglobulinemia Wart anogenital Wart common (NOS) Wart digitate Wart filiform Wart flat Wart genital Wart mosaic Wart Murray Williams Wart musician's Wart peruvian Wart plane Wart plantar Wart prosector's Wart seborrheic Wart senile Wart virus (NOS) Warty dyskeratoma Warty epidermal nevus Warty tuberculosis Wasp sting Water itch Waterhouse-Friderichsen syndrome Watson's syndrome Wax in ear Weary Kindler syndrome Webbing of neck Weber Christian disease Weber Cockayne syndrome Wegener's granulomatosis Weil's disease Wells' syndrome Wen Werlhof's disease Werner's syndrome West Nile fever Wet beriberi Wet gangrene of feet diabetic Wheal Whipple's disease Whipworm disease White finger vibration White folded gingivo-stomatosis White leg non-puerperal White nails in liver disease White piedra White sponge nevus White spot disease Whitehead Whitlow Whitlow herpetic Wiedemann Rautenstrauch syndrome Wild fire Wilkinson Sneddon syndrome Wilson's disease Wilson's lichen ruber Winchester syndrome Winter dermatitis Winter erythema keratolytic Winter itch Wiskott-Aldrich syndrome Witchcraft syndrome Witcop Brearley gentry syndrome Woodcutter's eczema Woolly hair nevus Woringer Kolopp disease Wound abscess Wound myiasis Wound open Wrinkle(s) Wrinkling finger Wrinkly skin syndrome Wyburn Mason syndrome Return to Alphabetical listing...

86. Waardenberg's/Waardenburg's Syndrome Home Page Waardenberg's/waardenburg's syndrome Home Page. Hello there! My name is GinaLynn, and I was diagnosed with Waardenberg's syndrome in Oct./Nov. of 2000. http://www.webspawner.com/users/waardenbergsyndrome/

Waardenberg's/Waardenburg's Syndrome Home Page Hello there! My name is Gina Lynn, and I was diagnosed with Waardenberg's Syndrome in Oct./Nov. of 2000. I am one of the lucky ones who has no hearing loss, but I do have Endolymphatic Hydrops (ELH). Symptoms of which can be: dizziness/vertigo, nausea, tinnitis (ringing in ears), extreme sensitivity to loud noises/bright lights/rapid air pressure changes/rapid increases in atmospheric moisture, depression, panic/anxiety attacks, poor depth perception (or spacial orientation), pain/fullness/popping/moisture/itching in ears, seeing things moving at the corners of the eyes that aren't really there, mental confusion/fogginess, a feeling that things are somehow "unreal or dreamlike", eyestrain, difficulties with speech and concentration, headaches, feeling off-balance or that the ground is moving or tilting, severe muscle pains in legs/ankles/feet, etc. Flags particular to Waardenberg Syndrome ONLY can be: hearing loss (sometimes, not always), different colored eyes (heterochromia - usually one blue, one brown) or unusually brilliant blue eyes, premature graying (hair/eyelashes), white forelocks, hair loss, broad nasal bridge, widely-spaced inside corners of eyes, eyebrows that grow together, vitiligo (depigmentation/white patches of skin), severe PMS- or peri-menopausal-like symptoms. On rare occasions, WS has been associated with other conditions that are present at birth, such as intestinal disorders (such as Hirschsprung's), elevation of the shoulder blade and disorders of the spine. A facial abnormality, known as cleft lip and/or palate, also has been associated with WS. There are at least four types of WS that are determined by which of the markers one exibits.

87. Waardenburg's Syndrome Type I Associated... waardenburg's syndrome type I associated with primary anetoderma. We report acase of waardenburg's syndrome type I associated with primary Anetoderma. http://www.imbiomed.com.mx/CDP/CDv5n3/english/Zcd63-08.html

Villanueva CE, Cruz BDJ, Ramos-GA Síndrome de Waardenburg tipo I Comunicación de un caso y breve revisión del tema Rev Cent Dermatol Pascua Waardenburg's syndrome type I associated with primary anetoderma. A case report and brief review of the literature ABSTRACT We report a case of Waardenburg's Syndrome type I associated with primary Anetoderma. Clinical and hystologic features confirmad the diagnosis.. Key words: Waerdenburg's Syndrome type I, Primary Anetoderma. Return to index H O M E Solicitude of articles

88. Waardenberg's/Waardenburg's Syndrome - HealthBoards Bulletin Board Message Reply w/Quote Though I have never actually been diagnosed,I'm sure I have a form of waardenburg's syndrome. I have an eye http://www.healthboards.com/ubb/Forum72/HTML/000073.html

Click Here to Visit our Sponsor FREE HealthBoards.com info from vendors! Select: Signup Inner Ear Disorders - new products and services Aging Alternative Medicine Back Care Beauty Free Stuff Health Products Herbal Products Natural Healing Nutrition Pain Mgmt Quit Smoking Sexuality Skin Care Stress Mgmt Viagra Vitamins Weight Loss Yoga Many more topics available! Enter your email address: Enter your zip/postal code: Click here to go to our old site message board - Inner Ear Disorders HealthBoards Bulletin Board Inner Ear Disorders Waardenberg's/Waardenburg's Syndrome profile register preferences faq ... next oldest topic Author GinaLynn Junior Member Posts: 8 From: Registered: Jan 2001 posted 06-19-2001 05:27 PM Hi. I have this rare genetic disorder. Common flags for Waardenberg's are premature graying, white forelocks, eyebrows that grow together, one blue eye or different-colored eyes. Less common flags are vitiligo, chronic constipation, spinal inflammation. One of the conditions that goes with Waardenberg's and is shared by persons with Meniere's is Endolymphatic Hydrops. Symptoms of which include tinnitus, pressure in ears, ear pain, dizziness/vertigo, sensitivity to loud sounds/bright lights, poor depth perception, nausea, panic attacks, depression, headaches, confusion, difficulty speaking, etc. Feel free to contact me with any questions.

89. Waardenburg's Syndrome - General Practice Notebook Notebook. waardenburg's syndrome. waardenburg's syndrome is the associationof patchy depigmentation of the skin; sensorineural deafness; http://www.gpnotebook.co.uk/cache/-1462763481.htm

Waardenburg's syndrome Waardenburg's syndrome is the association of: patchy depigmentation of the skin sensorineural deafness a white forelock unusual facial hair distribution - fusion of the eyebrows in the midline heterochromia of the iris bilateral displacement of the medial canthi Click here for more information...

90. Atmedica - WAARDENBURG (SYNDROME DE) Translate this page waardenburg's syndrome) syndrome génotypique caractérisé par une surdimutité,une hétérochromie de l'iris, des anomalies morphologiques des paupières http://www.atmedica.com/article/affichage/1,1039,A-parrubriques---34-34-103-2609

91. The Dictionary Of Cell And Molecular Biology - Online! waardenburg's syndrome. Autosomal dominant disorder with deafness and pigmentarydisturbances probably as a result of defects in function of neural crest. http://www.mblab.gla.ac.uk/~julian/dict2.cgi?6958

92. Types Of Deafness There are also syndromes associated with deafness, such as Treacher Collinssyndrome and waardenburg's syndrome. BACK TO TOP. waardenburg's syndrome. http://www.ndcs.org.uk/ch_deaf/chitypes.htm

93. Craniofacial Continuing Education - Parentpals.com Special Education Guide waardenburg's syndrome. Author Alice Kahn, Ph.D. COMING 2002, 2.3 What is a phenotype?2.4 What is waardenburg's syndrome (WS)? 2.4.1 Who discovered WS? http://www.parentpals.com/7.0continuinged/2002/Waardenburg.html

Special Education Continuing Education Waardenburg's Syndrome Author: Alice Kahn, Ph.D. COMING 2002 COURSE DESCRIPTION Introductory Level, Professional. It provides basic information about the birth anomalies called cleft lip and cleft palate, the processes of normal and abnormal velopharyngeal closure as well as the incidence and etiology. Participants will also learn to distinguish between overt clefts, and subtle conditions of occult and submucous cleft palate. See course outline below. LEARNER OUTCOMES To be determined at a later date. AUTHOR Alice Kahn, Ph.D. is an Associate professor of Speech Pathology in the Department of communication at Miami University in Oxford, Ohio. She received her master's degree from the University of Houston, and a doctoral degree from the University of Memphis. Dr. Kahn's current research and clinical interests focus on diagnosis and treatment of Waardenburg's syndrome; use of technology in clinical teaching; and patient literacy and readability of educational materials. Dr. Kahn is the author of

94. DJO Grand Rounds - Shiuey waardenburg's syndrome. These symptoms were not believed to be associatedwith his incidental diagnosis of waardenburg's syndrome. http://www.djo.harvard.edu/meei/GR/Shiuey030497/Shiuey030497Dx.html

Waardenburg's Syndrome Our patient's symptoms and complete neuro-ophthalmic examination were felt to be consistent with migraine headaches. These symptoms were not believed to be associated with his incidental diagnosis of Waardenburg's syndrome. When asked if he was diagnosed with this condition before, he replied that he may have recalled a physician using that term when he was a teenager. The clinical entity of Waardenburg's syndrome was first described in 1951. In the original description this syndrome consisted of developmental abnormalities in the eyelids, eye brows, nose-root, associated with pigmentary defects of the irides and head hair and congenital deafness. One of the cardinal findings of Waardenburg's syndrome is iris heterochromia. It is believed that this condition produces hypo-pigmentation of the affected iris as opposed to hyper-pigmentation. The evidence for this is the striking observation that patients with Waardenburg's syndrome of African descent have blue irides. Some patients may have hypo-chromic irides bilaterally without heterochromia. Hypopigmentation of the fundi may also be present. Pigmentatry abnormalities of the hair and skin are another prominent feature of this syndrome. Classically, there is a white forelock of hair (which this patient had as a teenager), but premature graying of hair and patches of white body hair are also very common. Well circumscribed hypo-pigmentation of the skin may also be found and is termed leucism. Other hair abnormalities in Waardenburg's include fusion of the eyebrows (synophrys).

95. OMIM ENTRY 193500 Online Mendellian Inheritance in Man details the clinical and genetic features of the disorder and its variants. Includes references. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?193500

96. Untitled Document http://dnalab-www.uia.ac.be/dnalab/hhh/syndromi.html

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