Familial Deafness

Common Name(s)

Familial Deafness

Description for this condition is not yet available.
 

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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 16 free, full-text research articles on human participants. First 3 results:

Familial clustering of congenital deafness, patent ductus arteriosus, Eisenmenger complex, and differential cyanosis: A case report.
 

Author(s): Ting-Wei Lin, Chih-Wei Tseng, Chi-Yao Huang, Kuo-Yang Wang, Kae-Woei Liang

Journal: Medicine (Baltimore). 2017 Jun;96(24):e7105.

 

Few studies had reported syndromes that include patent ductus arteriosus (PDA) with Eisenmenger syndrome and congenital deafness clustered in male siblings without facial, skeletal, or mental abnormalities.

Last Updated: 14 Jun 2017

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Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome.
 

Author(s): Li Wang, Qiong-Fen Lin, Hong-Yang Wang, Jing Guan, Lan Lan, Lin-Yi Xie, Lan Yu, Ju Yang, Cui Zhao, Jin-Long Liang, Han-Lin Zhou, Huan-Ming Yang, Wen-Ping Xiong, Qiu-Jing Zhang, Da-Yong Wang, Qiu-Ju Wang

Journal: Chin. Med. J.. 2017 Mar;130(6):703-709.

 

Hypoparathyroidism-deafness-renal dysplasia (HDR) syndrome is an autosomal dominant disorder primarily caused by haploinsufficiency of GATA binding protein 3 (GATA3) gene mutations, and hearing loss is the most frequent phenotypic feature. This study aimed at identifying the causative ...

Last Updated: 17 Mar 2017

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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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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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Clinical Trial Information This information is provided by ClinicalTrials.gov

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