Mohr-Tranebjaerg syndrome

Common Name(s)

Mohr-Tranebjaerg syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Mohr-Tranebjaerg syndrome" 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 "Mohr-Tranebjaerg syndrome" returned 2 free, full-text research articles on human participants. First 3 results:

Otopathology in Mohr-Tranebjaerg syndrome.
 

Author(s): Fayez Bahmad, Saumil N Merchant, Joseph B Nadol, Lisbth Tranebjaerg

Journal: Laryngoscope. 2007 Jul;117(7):1202-8.

 

Mohr-Tranebjaerg syndrome (MTS) is an X-linked, recessive, syndromic sensorineural hearing loss (HL) characterized by onset of deafness in childhood followed later in adult life by progressive neural degeneration affecting the brain and optic nerves. MTS is caused by mutations in ...

Last Updated: 2 Jul 2007

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Full-field electroretinograms in a family with Mohr-Tranebjaerg syndrome.
 

Author(s): V Ponjavic, S Andreasson, L Tranebjaerg, H A Lubs

Journal: Acta Ophthalmol Scand. 1996 Dec;74(6):632-5.

 

A family with a newly detected X-linked syndrome including sensorineural deafness, mental retardation, dystonia and blindness was examined with full-field electroretinography in order to order to find out if the blindness was caused by a retinal degeneration. Six affected males and ...

Last Updated: 31 Mar 1997

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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 "Mohr-Tranebjaerg syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Decision Support for Parents Receiving Information About Child's Rare Disease
 

Status: Recruiting

Condition Summary: Disorder of Sex Development; Intersex Conditions; Congenital Adrenal Hyperplasia; Hypospadias

 

Last Updated: 30 Jul 2015

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Aneuploidies in Embryos and Spermatozoa From Patients With Y-chromosome Microdeletions
 

Status: Not yet recruiting

Condition Summary: Male Sterility Due to Y-chromosome Deletions

 

Last Updated: 17 Aug 2015

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RA-2 13-cis Retinoic Acid (Isotretinoin)
 

Status: Recruiting

Condition Summary: Male Infertility; Klinefelter's Syndrome; Y-chromosome Microdeletions

 

Last Updated: 4 Aug 2015

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