Progressive Deafness: Causes & Reasons

Possible Causes for Progressive Deafness

progressive sensorineural deafness, Corneal dystrophy and sensorineural prelingual deafness, Harboyan syndrome. [link.springer.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

Autosomal-dominant forms of deafness are usually post-lingual and progressive. [genome.jp]

Bilateral Sensorineural Hearing Loss

Title Other Names: Gingival fibromatosis with progressive deafness; GFD; Gingival fibromatosis with sensorineural hearing loss; Gingival fibromatosis with progressive deafness [rarediseases.info.nih.gov]

“Jones Syndrome (Gingival Fibromatosis with Progressive Deafness)” [14612] �The statements on this Web site have not been evaluated by the Food and Drug Administration (FDA [wellnessadvocate.com]

GFD; Gingival fibromatosis with sensorineural hearing loss; Familial gingival fibromatosis associated with progressive deafness See More Categories: Jones syndrome is a [rarediseases.info.nih.gov]

Deafness, Autosomal Dominant 23

Symptoms - Deafness- autosomal dominant nonsyndromic sensorineural 23 Progressive deafness Causes - Deafness- autosomal dominant nonsyndromic sensorineural 23 Not supplied [checkorphan.org]

[…] variants in syndromic deafness, such as Jervell and Lange-Nielsen (hearing impairment and LQT), USH (deaf and progressive retinal pigmentosa), Biotinidase deficiency (Biotin [otogenetics.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [ipfs.io]

Other Acquired Abnormality of Ear Ossicles

Deafness, Progressive, with Stapes Fixation. Online Mendelian Inheritance in Man (OMIM). 1996; Bozorg Grayeli A. Progressive deafness with stapes fixation. [rarediseases.info.nih.gov]

MalaCards based summary : Deafness, Progressive, with Stapes Fixation, is also known as progressive deafness with stapes fixation. [malacards.org]

PubMed is a searchable database of medical literature and lists journal articles that discuss Progressive deafness with stapes fixation. [rarediseases.info.nih.gov]

Melhem-Fahl Syndrome

[…] familial epilepsy Myoclonus cerebellar ataxia deafness Myoclonus epilepsy partial seizure Myoclonus hereditary progressive distal muscular atrophy Myoclonus progressive epilepsy [mindmappedia.com]

deafness Macrothrombocytopenia with leukocyte inclusions Macu Macular corneal dystrophy Macular degeneration juvenile Macular degeneration, age-related Macular degeneration [statemaster.com]

deafness Macules hereditary congenital hypopigmented and hyperpigmented Madokoro Ohdo Sonoda syndrome Magnesium defect in renal tubular transport of Magnesium wasting renal [en.wikipedia.org]

Autosomal Dominant Deafness 11

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

Progressive deafness. Amyloidosis of AA type causing renal failure. [academic.oup.com]

Autosomal Recessive Deafness 42

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

UniProtKB/Swiss-Prot : 76 Deafness, autosomal recessive, 42: A prelingual, non-progressive form of non-syndromic sensorineural hearing loss. [malacards.org]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

Autosomal Dominant Deafness 64

Progressive deafness. Amyloidosis of AA type causing renal failure. [academic.oup.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

X-linked 4 XLD 0 TECTA 602574 Deafness, autosomal dominant 8/12; deafness type 21 AD, AR 23 TJP2 607709 Hypercholanemia, familial; Cholestasis, progressive familial intrahepatic [centogene.com]

Muckle-Wells Syndrome

Progressive sensorineural deafness, and, in approximately one third of the patients, amyloidosis of the kidneys as well as of other organs may occur. [ncbi.nlm.nih.gov]

We report the case of a 36-year-old man suffering since birth from a nonpruritic generalized urticaria, with inflammatory flares, joint manifestations and progressive deafness [karger.com]

Progressive nerve deafness develops subsequently, and, after several years, the disease is complicated by multiorgan AA-type amyloidosis (i.e., amyloidosis derived from the [ncbi.nlm.nih.gov]

Autosomal Recessive Deafness 22

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

Deafness is non-syndromic, sensorineural, and progressive. [academic.oup.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

Mohr Syndrome

Progressive deafness occurs at age 3 to 5 years. [accessanesthesiology.mhmedical.com]

Acronym MTS Synonyms DDS DFN-1 Dystonia-deafness syndrome Jensen syndrome Opticoacoustic nerve atrophy with dementia X-linked progressive deafness type 1 Keywords Any medical [uniprot.org]

Syndrome MOHR-TRANEBJAERG SYNDROME; MTS DDON syndrome Deafness Syndrome, Progressive, With Blindness, Dystonia, Fractures, and Mental Deficiency Dystonia-Deafness Syndrome [wikidata.org]

Usher Syndrome Type 1

A slowly progressive deafness has been identified in one subgroup of Usher patients (gene USH3A ) due to mutations in clarin-1, a transmembrane protein with a possible role [aao.org]

Hearing loss usually presents first, although the speed of progression to deafness can vary greatly between individuals. [news-medical.net]

[…] and progressive retinitis pigmentosa. [eric.ed.gov]

Usher Syndrome Type 1D

A slowly progressive deafness has been identified in one subgroup of Usher patients (gene USH3A ) due to mutations in clarin-1, a transmembrane protein with a possible role [aao.org]

Overview A rare inherited disorder characterized by sensorineural deafness and progressive vision loss which starts during the first decade of life and blindness usually occurs [checkorphan.org]

Disease Overview Usher syndrome is a genetic disorder characterized by sensorineural hearing loss or deafness and progressive vision loss due to retinitis pigmentosa. [rarediseases.org]

Malignant Hyperthermia - Arthrogryposis - Torticollis

[…] familial epilepsy Myoclonus ataxia Myoclonus cerebellar ataxia deafness Myoclonus epilepsy partial seizure Myoclonus hereditary progressive distal muscular atrophy Myoclonus [en.wikipedia.org]

[…] familial epilepsy Myoclonus ataxia Myoclonus cerebellar ataxia deafness Myoclonus epilepsy partial seizure Myoclonus epilepsy Myoclonus hereditary progressive distal muscular [thefullwiki.org]

Macrothrombocytopenia progressive deafness[?] Macrothrombocytopenia with leukocyte inclusions[?] Macular corneal dystrophy[?] Macular degeneration juvenile[?] [encyclopedia.kids.net.au]

Neonatal Adrenoleukodystrophy

See Leukodystrophy. a·dre·no·leu·ko·dys·tro·phy (ALD) ( ă-drē'nō-lū'kō-dis'trŏ-fē ) Rare disease of the central nervous system characterized by progressive blindness, deafness [medical-dictionary.thefreedictionary.com]

Vision and hearing dysfunction are progressive and result in blindness and deafness. Osteoporosis and fractures can occur in patients who are less mobile. [orpha.net]

[…] skin pigmentation, and progressive dementia. [medical-dictionary.thefreedictionary.com]

Autosomal Recessive Deafness 44

Gingival fibromatosis with progressive deafness syndrome Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Hereditary essential tremor Hereditary [icdlist.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

A follow-up study in a family with dominant progressive inner ear deafness. [nejm.org]

Fazio-Londe Disease

• Among the hereditary affections of the nervous system associated with deafness, a rare condition called "progressive pontobulbar palsy with deafness" has been described. [jamanetwork.com]

The remaining 3 patients had no deafness, although likewise manifested subacute progressive ponto-bulbar palsy. [uniprot.org]

The disease is characterized by progressive sensorineural deafness, bulbar palsy, and respiratory compromise. 1 The age of onset varies from 0.3–17 years, with a mean age [nature.com]

Autosomal Recessive Deafness 88

Three brothers presented with bilateral and non-syndromal progressive deafness in early teenage. [webview.isho.jp]

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

Autosomal Recessive Deafness 24

Autosomal dominant nonsyndromic hearing loss (DFNA65), also caused by a TBC1D24 mutation, is characterized by slowly progressive deafness affecting initially the high frequencies [epilepsygenetics.net]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

AD/AR 36 120 TJP2 Cholestasis, progressive familial intrahepatic, Hypercholanemia, familial, Deafness, autosomal dominant 51 AD/AR 25 27 TMC1 Deafness, Deafness, autosomal [blueprintgenetics.com]

Retinohepatoendocrinologic Syndrome

[…] nerve deafness Renal tubular acidosis, distal Renal tubular acidosis, distal, autosomal dominant Renal tubular acidosis, distal, autosomal recessive Renal tubular acidosis [mindmappedia.com]

[…] nerve deafness Renal tubular acidosis, distal, autosomal dominant Renal tubular acidosis, distal, autosomal recessive Renal tubular acidosis, distal, type 3 Renal tubular [fact-index.com]

[…] anomalies Renal glycosuria Renal h-Renal t Renal hepatic pancreatic dysplasia Dandy Walker cyst Renal hypertension Renal osteodystrophy Renal rickets Renal tubular acidosis progressive [ssf.f15ijp.com]

Congenital Deafness

Atopic dermatitis and perceptive, non-progressive congenital deafness might be genetically associated. [ncbi.nlm.nih.gov]

Four members of a family had the heriditary syndrome of dominantly inherited progressive optic atrophy and congenital sensorineural deafness. [ncbi.nlm.nih.gov]

deafness. [symptoma.com]

Autosomal Dominant Deafness 9

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

deafness (DFNA20/26). [genome.jp]

High Myopia-Sensorineural Deafness Syndrome

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

Therefore, whenever a child presents with episodic or progressive ataxia and progressive sensorineural deafness, with or without neurologic or cutaneous symptoms, biotinidase [quizlet.com]

Children are born with hearing dysfunction called sensorineural deafness that progresses to a complete hearing loss. [medigoo.com]

Mononen-Karnes-Senac Syndrome

Autosomal Dominant Deafness 33

Progressive Deafness-Dystonia due to SERAC1 Mutations: A study of 67 cases. Ann Neurol 2017:82:1004-1015 Mafong DD and others. [dizziness-and-balance.com]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

[…] of human deafness. [karger.com]

Autosomal Recessive Deafness 1B

For the autosomal dominant forms of deafness, mutations in the COCH gene result in progressive postlingual deafness associated with severe attacks of vertigo and subjective [orpha.net]

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

X-linked 4 XLD 0 TECTA 602574 Deafness, autosomal dominant 8/12; deafness type 21 AD, AR 23 TJP2 607709 Hypercholanemia, familial; Cholestasis, progressive familial intrahepatic [centogene.com]

Autosomal Recessive Deafness 103

This type of deafness is not inherited from fathers. Late onset progressive deafness is the most common neurological disability of the elderly. [en.wikipedia.org]

AD/AR 36 120 TJP2 Cholestasis, progressive familial intrahepatic, Hypercholanemia, familial, Deafness, autosomal dominant 51 AD/AR 25 27 TMC1 Deafness, Deafness, autosomal [blueprintgenetics.com]

[…] in only one instance. 8 This latter heterozygous GJB2 mutation (W44C), which is associated with profound prelingual and progressive non-syndromic deafness, lies in the E1 [jmg.bmj.com]

Richards-Rundle Syndrome

Aminoglycosides should be used carefully in presence of progressive deafness and renal dysfunction. [accessanesthesiology.mhmedical.com]

deafness myoclonus mental deterioration, hearing loss, and nephropathy autosomal dominant trait myoclonus ataxia hearing loss Congenital deafness mild chronic epilepsy of [brainscape.com]

Very few patients have been reported with ADR Syndrome, the characteristic features of the condition being mental retardation, deafness, ataxia, developmental delay and progressive [cags.org.ae]

Usher Syndrome Type 1J

Hearing loss usually presents first, although the speed of progression to deafness can vary greatly between individuals. [news-medical.net]

Usher Syndrome is a genetic condition characterized by deafness at birth or progressive hearing loss and progressive vision loss. [usher1f.org]

Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction. [usherkidsuk.com]

Woodhouse-Sakati Syndrome

[…] disability syndrome Extrapyramidal Disorder, Progressive, With Primary Hypogonadism, Mental Retardation, and Alopecia Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation [wikidata.org]

[…] mellitus and progressive extrapyramidal defects. [ncbi.nlm.nih.gov]

Woodhouse–Sakati Syndrome (WSS) is a rare autosomal recessive multisystemic disorder that is marked by hypogonadism, alopecia, intellectual disability, deafness, diabetes [agris.fao.org]