<--- Back to Details
First PageDocument Content
Channelopathy / Sensorineural hearing loss / Mitochondrial diseases / Congenital hearing loss / Rare diseases / Nonsyndromic deafness / Hearing impairment / Pendred syndrome / Treacher Collins syndrome / Health / Deafness / Syndromes
Date: 2008-03-12 11:18:28
Channelopathy
Sensorineural hearing loss
Mitochondrial diseases
Congenital hearing loss
Rare diseases
Nonsyndromic deafness
Hearing impairment
Pendred syndrome
Treacher Collins syndrome
Health
Deafness
Syndromes

Physician ethics and genetic testing

Add to Reading List

Source URL: www.peds.ufl.edu

Download Document from Source Website

File Size: 94,48 KB

Share Document on Facebook

Similar Documents

Mitochondrial diseases / Mitochondrial genetics / Molecular biology / Mitochondrion / Mitochondrial DNA / Genetic disorder / Human mitochondrial genetics / MELAS syndrome

What are mitochondria? Mitochondria are often called the ‘cell’s powerhouse.’ They are specialized compartments within almost every cell. They are responsible for producing 90% of the energy needed by our body to s

DocID: 1mBCG - View Document

Nonsyndromic deafness / Biology / Genetics / Sensorineural hearing loss / Health / GJB2 / GJB6 / Philosophy of biology / Mutation / Deafness / Mitochondrial diseases / Channelopathy

Microsoft Word - 3 R.S.R.

DocID: 17IJX - View Document

Mitochondrial disease / Mitochondrion / Non-Mendelian inheritance / Mutation / Mitochondrial DNA / Human genome / Chromosome / Duchenne muscular dystrophy / Genetic testing / Biology / Genetics / Genetic disorder

Facts About Genetics and Neuromuscular Diseases

DocID: 14w4V - View Document

Organelles / Genetics / Genetic disorder / Mitochondrial diseases / Biology / Cellular respiration / Mitochondrion

Preventing incurable genetic disease Mitochondrial replacement offers a route to the prevention of life-limiting genetic disease. However, this procedure involves manipulations of traditional genetic inheritance. It has

DocID: 11Koj - View Document

DNA / Spindle transfer / Mitochondrial diseases / Genetic genealogy / Mitochondrion / Mitochondrial DNA / Human Fertilisation and Embryology Authority / Mitochondrial Eve / Cell / Biology / Genetics / Mitochondrial genetics

Q&A: Mitochondrial Donation About 1 in 200 children in the UK carry a mitochondrial DNA mutation, while around 1 in 6500 children is thought to develop serious mitochondrial disease. The Wellcome Trust Centre for Mitocho

DocID: 11oJf - View Document