Familial Deafness

Common Name(s)

Familial Deafness

Description for this condition is not yet available.
 

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Condition Specific Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Familial Deafness" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Familial Deafness" returned 13 free, full-text research articles on human participants. First 3 results:

The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy.
 

Author(s): Claudia Izzi, Pietro Maffei, Gabriella Milan, Regina Tardanico, Paolo Foini, Jan Marshall, Alessandra Marega, Francesco Scolari

Journal: Kidney Int.. 2011 Mar;79(6):691-2.

 

Last Updated: 1 Mar 2011

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Coexistent MEFV and CIAS1 mutations manifesting as familial Mediterranean fever plus deafness.
 

Author(s): Davinder Singh-Grewal, Jeffrey Chaitow, Ivona Aksentijevich, John Christodoulou

Journal: Ann. Rheum. Dis.. 2007 Nov;66(11):1541.

 

Last Updated: 15 Oct 2007

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Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.
 

Author(s): C Le Caignec, M Lefevre, J J Schott, A Chaventre, M Gayet, C Calais, J P Moisan

Journal: Am. J. Hum. Genet.. 2002 Jul;71(1):180-6.

 

In the present study, we report a kindred with hearing loss, congenital heart defects, and posterior embryotoxon, segregating as autosomal dominant traits. Six of seven available affected patients manifested mild-to-severe combined hearing loss, predominantly affecting middle frequencies. ...

Last Updated: 17 Jun 2002

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Familial Deafness" returned 1 free, full-text review articles on human participants. First 3 results:

Familial idiopathic hypoparathyroidism, sensorineural deafness and renal dysplasia.
 

Author(s): S Ishida, H Isotani, K Kameoka, T Kishi

Journal: Intern. Med.. 2001 Feb;40(2):110-3.

 

We describe a 27-year-old woman with familial idiopathic hypoparathyroidism, bilateral sensorineural deafness and right renal aplasia. There was a family history of deafness in her father and two other family members with sensorineural deafness, one of whom had hypoparathyroidism. ...

Last Updated: 12 Apr 2001

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Alport Syndrome Treatments and Outcomes Registry
 

Status: Recruiting

Condition Summary: Alport Syndrome

 

Last Updated: 3 Sep 2014

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