reduced results from

155 B

16 M

2 M

267

211

to ~30 options

options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications

category genetic or congenital, head and neck frequency rare (U.S.)

likelihood by age

likelyhood by duration of symptoms

related physician types family practitioner internist genetics specialist postal code Find Local The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.

congenital deafness syndromes - deafness associated with other abnormalities Definition for congenital deafness syndromes http://www.tchain.com/otoneurology/disorders/hearing/cong_hearing.html some common symptoms face deformities hearing loss some related diagnoses 1 - 7 of 30 diagnoses fetal alcohol syndrome Turner's Syndrome thalassemia intermedia nasal polyp neurofibromatosis type 1 relapsing polychondritis syphilis   more do i have 'congenital deafness syndromes'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'congenital deafness syndromes' 1 - 3 of 3 diagnostic tests Molecular Genetic Studies congenital deafness syndromes and Molecular Genetic Studies Hearing test standard technique of representing hearing loss congenital deafness syndromes and Hearing test speech reception threshold (SRT) congenital deafness syndromes and speech reception threshold (SRT) therapeutic procedures for 'congenital deafness syndromes'? 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 congenital deafness syndromes: therapeutic procedure search results for 'congenital deafness syndromes' 1 - 2 of 2 therapeutic procedures rankings are computer generated. please consult your health care provider. Hearing aids instruments to enable a person to hear congenital deafness syndromes and Hearing aids Speech Therapy congenital deafness syndromes and Speech Therapy medications search results for 'congenital deafness syndromes' rankings are computer generated. please consult your health care provider. web search results for congenital deafness syndromes Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - congenital deafness syndromes Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF. ... with Tietz syndrome have congenital profound deafness and generalised ... anomalies and deafness, which characteristically have patchy depigmentation and ... http://www.ncbi.nlm.nih.gov/pubmed/10851256   www.ncbi.nlm.nih.gov - summary Congenital rubella syndrome - Wikipedia, the free encyclopedia The classic triad for congenital rubella syndrome is: Sensorineural deafness - (58% of patients) ... · Rubella virus (Rubella, Congenital rubella syndrome) ... http://en.wikipedia.org/wiki/Congenital_rubella_syndrome   en.wikipedia.org - summary EML1 - NextBio ... consisting of congenital deafness, retinitis pigmentosa, ... syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis ... http://www.nextbio.com/b/home/home.nb?q=Eml1   www.nextbio.com - summary Nonsyndromic deafness - Genetics Home Reference ... conductive hearing loss ; congenital ; connexin ; DNA ; gap junctions ; gene ; ... sex chromosomes ; sign ; stapes ; subunit ; symptom ; syndrome ; trait ... http://ghr.nlm.nih.gov/condition=nonsyndromicdeafness   ghr.nlm.nih.gov - summary WAARDENBURG SYNDROMES - Pedbase.org unilateral or bilateral sensorineural hearing loss or deafness ... congenital deafness (20%) 2. Type I (dystopia canthorum present) all features above ... http://pedbase.org/w/waardenburg-syndrome/   pedbase.org - summary Craniofacial Abnormalities: Congenital Craniofacial and Musculoskeletal ... Waardenburg's syndrome. Deafness, partial albinism (white forelock usually), heterochromic iris, ... Agenesis of the jaw: Congenital absence of the condyloid ... http://www.merck.com/mmpe/sec19/ch288/ch288d.html   www.merck.com - summary Jervell and Lange-Nielsen Syndrome ... the main title of the report Jervell and Lange - Nielsen Syndrome is not the name you expected. Please check the synonyms ... Deafness, Congenital, and ... http://www.webmd.com/a-to-z-guides/jervell-and-lange-nielsen-syndrome   www.webmd.com - summary Congenital heart disease ... and chromosomal syndromes such as Down syndrome, ... Deafness. Dermatology. Diabetes. Headaches. Heartburn. Heart Disease. Depression. IBS/Crohn's Disease ... http://adam.about.com/encyclopedia/infectiousdiseases/Congen...   adam.about.com - summary Deafness and Hereditary Hearing Loss Overview -- GeneReviews -- NCBI ... ... Pendred syndrome accounted for up to 7.5% of congenital deafness, but ... The syndrome consists of congenital deafness and prolongation of the QT interval ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=deafness-overview   www.ncbi.nlm.nih.gov - summary CDC - Newborn Screening for Congenital Infectious Diseases Microcephaly, intracranial calcifications, deafness, failure to thrive, HSMa ... 1 congenital rubella syndrome (died) 2 with scars in 1 eye ... http://www.cdc.gov/ncidod/EID/vol10no6/03-0830.htm   www.cdc.gov - summary Orphanet: Waardenburg syndrome type 2 The portal for rare ... Waardenburg syndromes are deafness syndromes associated with ... history of congenital deafness or pigmentation anomalies ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=895   www.orpha.net - summary Craniofacial Abnormalities: Congenital Craniofacial and Musculoskeletal ... Waardenburg's syndrome. Deafness, partial albinism (white forelock usually), heterochromic iris, ... Congenital absence of the condyloid process (and sometimes ... https://www.merck.com/mmpe/print/sec19/ch288/ch288d.html   /www.merck.com - summary Nonsyndromic Hearing Loss and Deafness, DFNB1 -- GeneReviews -- NCBI ... Keratitis-ichthyosis-deafness (KID) syndrome is an ectodermal dysplasia in which ... Jervell and Lange-Nielsen syndrome (JLNS) includes congenital profound bilateral ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=dfnb1   www.ncbi.nlm.nih.gov - summary MedlinePlus: Usher Syndrome ... Syndrome(National Eye Institute, National Institute on Deafness and ... Article: Usher syndrome and Leber congenital amaurosis are molecularly linked via... http://www.nlm.nih.gov/medlineplus/ushersyndrome.html   www.nlm.nih.gov - summary Cockayne syndrome - Genetics Home Reference Dwarfism-retinal atrophy-deafness syndrome. Progeria-Like Syndrome. progeroid nanism ... cancer ; cataract ; cell ; congenital ; DNA ; DNA damage ; dwarfism ; ... http://ghr.nlm.nih.gov/condition=cockaynesyndrome   ghr.nlm.nih.gov - summary Deafness and Hereditary Hearing Loss Overview ... that Pendred syndrome accounted for up to 7.5% of congenital deafness, ... The syndrome consists of congenital deafness and prolongation of the QT interval ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Renal Cystic Disease in Malformation Syndromes: Cystic Kidney Disease ... Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia ... Introduction· Acquired Renal Cysts· Congenital Renal Cystic Dysplasia· Medullary ... http://merck.com/mmpe/sec17/ch232/ch232g.html   merck.com - summary [Ichthyosis hystrix gravior typus Rheydt: an otologic-dermatologic ... Deafness/complications* Deafness/congenital. Deafness/diagnosis. Dermatomycoses ... Ichthyosis/congenital. Ichthyosis/pathology. Male. Skin/pathology. Syndrome ... http://www.ncbi.nlm.nih.gov/pubmed/145534   www.ncbi.nlm.nih.gov - summary Congenital Renal Cystic Dysplasia: Cystic Kidney Disease: Merck Manual ... Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia. Dysmenorrhea. Dyspepsia ... see Congenital Renal and Genitourinary Anomalies: Prune-Belly Syndrome) ... http://www.merck.com/mmpe/sec17/ch232/ch232c.html   www.merck.com - summary Albinism - Yahoo! Health Black Locks-Albinism-Deafness of Sensoneural Type (BADS) Ocular Albinism ... The syndromes of this disorder are categorized as Tyrosinase-Negative ... http://health.yahoo.com/other-other/albinism/healthwise--nord42.html   health.yahoo.com - summary Kidneys and urinary system - Genetics Home Reference congenital hereditary hematuria see ... congenital hemorrhagic nephritis see Alport syndrome ... urticaria-deafness-amyloidosis syndrome see Muckle ... http://ghr.nlm.nih.gov/conditionCategory=kidneysandurinarysystem   ghr.nlm.nih.gov - summary Congenital Diaphragmatic Hernia Overview callosum, hypertelorism, myopia, and sensorineural deafness syndrome) is a rare autosomal ... Congenital diaphragmatic hernia occurs as an isolated finding, as ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Introduction: Adrenal Disorders: Merck Manual Professional Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia. Dysmenorrhea. Dyspepsia ... Hyperfunction produces distinct clinical syndromes. ... http://www.merck.com/mmpe/sec12/ch153/ch153a.html   www.merck.com - summary Ocular Albinism, X-Linked -- GeneReviews -- NCBI Bookshelf ... skin, this syndrome consists of congenital deafness and vestibular dysfunction. ... syndrome, and supernormal rod response-type, as well as Leber ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=x-oa   www.ncbi.nlm.nih.gov - summary Medullary Sponge Kidney: Cystic Kidney Disease: Merck Manual Professional Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia. Dysmenorrhea ... Introduction· Acquired Renal Cysts· Congenital Renal Cystic Dysplasia·Medullary ... http://www.merck.com/mmpe/sec17/ch232/ch232d.html   www.merck.com - summary Townes-Brocks Syndrome - Genetics Home Reference Gene Review: Townes-Brocks Syndrome. MedlinePlus Encyclopedia: Ear Disorders (image) ... deafness-imperforate anus-hypoplastic thumbs syndrome ... http://ghr.nlm.nih.gov/condition=townesbrockssyndrome   ghr.nlm.nih.gov - summary Nonsyndromic Hearing Loss and Deafness, DFNB1 Hystrix-like ichthyosis-deafness (HID) syndrome is an autosomal dominant keratinizing ... Usher syndrome type I is characterized by a congenital, bilateral, profound ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Molecular basis of human Usher syndrome: deciphering the meshes of the ... In USH1 patients, congenital deafness is combined with a pre-pubertal onset of ... Deafness/congenital. Deafness/genetics. Disease Models, Animal. Dynein ... http://www.ncbi.nlm.nih.gov/pubmed/16545802   www.ncbi.nlm.nih.gov - summary Ventricular Tachycardia (VT): Arrhythmias and Conduction Disorders ... The long QT syndrome (congenital or acquired) is associated with a particular ... associated with congenital deafness and, in the past, was referred to as the ... http://www.merck.com/mmpe/print/sec07/ch075/ch075k.html   www.merck.com - summary Nonsyndromic Hearing Loss and Deafness, DFNA3 -- GeneReviews -- NCBI ... Keratitis-ichthyosis-deafness (KID) syndrome, an ectodermal dysplasia ... Waardenburg syndrome type 1 (WS1) is characterized by congenital sensorineural ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=dfna3   www.ncbi.nlm.nih.gov - summary Ocular Albinism, X-Linked biogenesis leading to congenital and persistent visual impairment ... skin, this syndrome consists of congenital deafness and vestibular dysfunction. In some ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Mutation of the EYA1 gene in patients with branchio-oto syndrome. ... with autosomal dominant hereditary deafness and congenital preauricular fistula. ... Oto-Renal Syndrome/genetics* Deafness/genetics. Female. Follow ... http://www.ncbi.nlm.nih.gov/pubmed/12701758   www.ncbi.nlm.nih.gov - summary Hearing impairment - Wikipedia, the free encyclopedia The congenital defect microtia can cause full or partial deafness depending upon ... Hearing loss with craniofacial syndromes. King-Kopetzky syndrome ... http://en.wikipedia.org/wiki/Hearing_impairment   en.wikipedia.org - summary Jervell and Lange-Nielsen Syndrome - Yahoo! Health ... the report Jervell and Lange-Nielsen Syndrome is not the name you expected. ... Deafness, Congenital, and Functional Heart Disease. Surdocardiac Syndrome ... http://health.yahoo.com/children-resources/jervell-and-lange...   health.yahoo.com - summary Genomics|HuGENet|Reviews|longQT syndrome|PubMed ID: 16540748 The mission of the National Office of Public Health Genomics is to integrate ... least likelihood, such as congenital deafness), based on personal and family ... http://www.cdc.gov/genomics/hugenet/reviews/longQT.htm   www.cdc.gov - summary The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic ... ... cutaneous (CFC) syndrome are autosomal dominant multiple congenital anomaly ... abnormal genitalia, retardation of growth, and sensorineural deafness) syndrome. ... http://www.ncbi.nlm.nih.gov/pubmed/18470943?ordinalpos=3&ito...   www.ncbi.nlm.nih.gov - summary Syrinx: Spinal Cord Disorders: Merck Manual Professional Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia ... For unknown reasons, these congenital abnormalities often expand during the teen ... http://www.merck.com/mmpe/sec16/ch224/ch224j.html   www.merck.com - summary Introduction: Pelvic Relaxation Syndromes: Merck Manual Professional Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia. Dysmenorrhea. Dyspepsia ... common factors include congenital malformations, increased abdominal ... http://www.merck.com/mmpe/sec18/ch250/ch250a.html   www.merck.com - summary Talk:Hearing impairment/Deafness - Wikipedia, the free encyclopedia Congenital - deafness at birth. Pre-lingual ? deafness beginning ... Congenital, profound, bilateral, sensorineural. Autosomal recessive. Pendred syndrome[12] ... http://en.wikipedia.org/wiki/Talk:Hearing_impairment/Deafness   en.wikipedia.org - summary Branchiootorenal Syndrome -- GeneReviews -- NCBI Bookshelf The BO syndrome is characterized by deafness, cup-ear deformity, preauricular ... Congenital conductive or mixed deafness, preauricular sinus, external ear ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bor   www.ncbi.nlm.nih.gov - summary Chromosomal Deletion Syndromes: Chromosomal Anomalies: Merck Manual ... Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia. Dysmenorrhea ... They tend to cause severe congenital anomalies and markedly retarded mental and ... http://www.merck.com/mmpe/sec19/ch294/ch294e.html   www.merck.com - summary Congenital Fibrosis of the Extraocular Muscles syndromes are characterized by congenital non-progressive ophthalmoplegia (inability to ... features include sensorineural and/or conductive deafness. Page 8 ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary SOX10 mutations in patients with Waardenburg-Hirschsprung disease. Waardenburg syndrome (WS; deafness with pigmentary abnormalities) and ... aganglionic megacolon) are congenital disorders caused by defective function of ... http://www.ncbi.nlm.nih.gov/pubmed/9462749   www.ncbi.nlm.nih.gov - summary Ayazi syndrome - Wikipedia, the free encyclopedia ... syndrome is a syndrome characterized by choroideremia, congenital deafness and obesity. ... obesity, and congenital deafness". Am J Ophthalmol ... http://en.wikipedia.org/wiki/Ayazi_syndrome   en.wikipedia.org - summary Cancer Medicine ... first of the multiple hamartoma syndromes to lend itself to genetic characterization. ... ear anomalies and deafness, congenital heart disease, and hypogonadism. ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=cmed6.section.4589#4590   www.ncbi.nlm.nih.gov - summary Donnai-Barrow Syndrome -- GeneReviews -- NCBI Bookshelf Diaphragmatic hernia-hypertelorism-myopia-deafness syndrome. Prevalence ... Donnai-Barrow syndrome (DBS) is associated with congenital diaphragmatic hernia ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai   www.ncbi.nlm.nih.gov - summary Deafblindness - Wikipedia, the free encyclopedia Some people have congenital deafness and acquired blindness (such as glaucoma or ... Congenital rubella syndrome. Tommy (rock opera) [edit] References ... http://en.wikipedia.org/wiki/Deafblindness   en.wikipedia.org - summary Carbohydrate Intolerance: Malabsorption Syndromes: Merck Manual ... Deafness, Sudden. Diarrhea (in GI) Diarrhea (in PED) Diplopia ... · Bacterial Overgrowth Syndrome·Carbohydrate Intolerance ... Congenital ... http://www.merck.com/mmpe/sec02/ch017/ch017c.html   www.merck.com - summary WFS1-Related Disorders -- GeneReviews -- NCBI Bookshelf ... congenital deafness to a milder, sometimes progressive sensorineural hearing impairment. ... Deafness-dystonia-optic neuronopathy syndrome (DDON, or Mohr ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=wfs   www.ncbi.nlm.nih.gov - summary David J Amor - NextBio ... Russell-Silver syndrome SCN5A sensorineural deafness tumour ... an apparently novel syndrome comprising obesity, congenital hypothyroidism, ... http://www.nextbio.com/b/literature/literature.nb?author=David+J+Amor   www.nextbio.com - summary show more 1  2