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388 Possible Causes for Family History of Deafness

  • Congenital Deafness

    Parents are strongly advised to be aware of their family history of deafness and immediately consult a medical professional, if their child does not appropriately respond[symptoma.com] The families were assessed for a history of syncope and deafness and underwent ECG evaluations regarding lengthened QTc interval.[link.springer.com] In the majority of cases, Congenital Deafness is caused by a genetic mutation of the connexin protein family. Diagnosis should start with an audiometric test.[symptoma.com]

  • Wolfram Syndrome

    , *Neurological signs (ataxia, epilepsy, neuropathy, cognitive impairment), *Renal tract abnormalities, *1 loss of function mutation in _WFS1/CISD2_ AND/OR family history[diapedia.org] Confirmation of the Diagnosis Although the medical and family histories and the findings of the physical examination are vital for the diagnosis of Wolfram syndrome, genetic[doi.org] Minor criteria Minimum required Other variable suggestive evidence: *Diabetes mellitus *Diabetes insipidus, *Diabetes mellitus 16 yrs, *Optic atrophy 16 yrs, *sensorineural deafness[diapedia.org]

  • Otosclerosis

    Patients with pure sensorineural loss with family history, age of onset, audiometric pattern and good auditory discrimination indicate the possibility of cochlear otosclerosis[drtbalu.co.in] Patients with surgically confirmed otosclerosis who show progressive sensorineural deafness disproportionate to age. 2.[drtbalu.co.in]

  • Alport Syndrome

    Two patients with recurrent haematuria but no family history of deafness or haematuria showed similar extensive changes and are regarded as new mutant cases of hereditary[ncbi.nlm.nih.gov] In contrast, family history of HN without nerve deafness, normal or nearly normal kidney on repeat biopsy, and thin or normal GBM by EM are suggestive of less or nonprogressive[ncbi.nlm.nih.gov] In any child or adolescent with persistent microscopic hematuria, carefully seek a family history of hematuria, early onset deafness, and renal insufficiency (especially in[emedicine.medscape.com]

  • Usher Syndrome Type 1

    In the early stages it may be thought of purely as an auditory problem and the problem of sight is not anticipated unless there is a family history.[patient.info] Right now, from family history and genetic evaluations, we do not always have the ability to identify the gene in a person.[audiologyonline.com] The other major cause of deafness and blindness is congenital rubella.[patient.info]

  • Hypertension

    View/Print Table TABLE 4 History Suggesting Possible Etiologies or Associations with Hypertension Possible etiology and/or associations Family history Cardiovascular disease[aafp.org] ., ma huang), and tobacco use. table 4 History Suggesting Possible Etiologies or Associations with Hypertension Possible etiology and/or associations Family history Cardiovascular[web.archive.org] […] stroke) Primary hypertension Deafness Congenital or familial renal disease Dyslipidemia Primary hypertension Endocrine problems (e.g., diabetes, thyroid, adrenal) Familial[aafp.org]

  • Essential Hypertension

    View/Print Table TABLE 4 History Suggesting Possible Etiologies or Associations with Hypertension Possible etiology and/or associations Family history Cardiovascular disease[aafp.org] […] stroke) Primary hypertension Deafness Congenital or familial renal disease Dyslipidemia Primary hypertension Endocrine problems (e.g., diabetes, thyroid, adrenal) Familial[aafp.org] (e.g., myocardial infarction, stroke) Primary hypertension Deafness Congenital or familial renal disease Dyslipidemia Primary hypertension Endocrine problems (e.g., diabetes[aafp.org]

  • Klein-Waardenburg Syndrome

    Prevention Genetic counseling may be valuable for prospective parents with a family history of Waardenburg syndrome.[dxline.info] Call for a hearing test if you or your child has deafness or decreased hearing. visHeader References Milunsky JM.[nicklauschildrens.org] Call your health care provider for a hearing test if you or your child has deafness or decreased hearing.[medlineplus.gov]

  • Kniest Dysplasia

    Kniest dysplasia is a severe chondrodysplasia caused by the defective formation of type II collagen. We report about Dr. Kniest, who first described the condition in 1952, and his patient, who, at the age of 50 years is severely handicapped with short stature, restricted joint mobility, and blindness but is mentally[…][ncbi.nlm.nih.gov]

  • Meniere's Disease

    People with a family history of Ménière’s disease are at a higher risk of developing this condition, however we do not know if it is truly an inherited condition.[my.clevelandclinic.org] […] individuals in the United States are currently diagnosed with Ménière’s disease, and about 45,500 cases are newly diagnosed each year, according to National Institute on Deafness[my.clevelandclinic.org]

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