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TMC1, a Deafness-Related Gene by nih.gov have discovered that dominant and recessive mutations in TMC1 underlie two forms of hereditary deafness, known... Relevant Publication: K Kurima et al. Dominant and recessive deafness caused by mutations of a novel...
Genetics Home Reference: congenital deafness with labyrinthine aplasia, microtia, and microdontia by nih.gov deafness with labyrinthine aplasia, microtia, and microdontia (also called LAMM syndrome) is a condition... of hearing loss called sensorineural deafness that is present from birth (congenital). Because the inner ear...
Genetics Home Reference: keratitis-ichthyosis-deafness syndrome by nih.gov disease, which is not a feature of the autosomal dominant form. The autosomal recessive condition... providers. Gene Tests: Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant...
Genetics Home Reference: hereditary sensory and autonomic neuropathy type IE by nih.gov use for hereditary sensory and autonomic neuropathy type IE? DNMT1-related dementia, deafness, and sensory... Reviewed November 2012 What is hereditary sensory and autonomic neuropathy...
Genetic deafness by Funny Old Life Healthy Living Professional months premature and stayed in an incubator for 3 months, so the cause of my deafness... of my deafness is therefore at a microscopic level, and decided to carry out genetic testing as a permanent...
Genetics Home Reference: anhidrotic ectodermal dysplasia with immune deficiency by nih.gov recessive or autosomal dominant. How common is anhidrotic ectodermal dysplasia with immune... in the IKBKG gene cause X-linked recessive EDA-ID, and mutations in the NFKBIA gene cause autosomal dominant...
Hot Off the Lab Bench: Research News on Hearing Loss, Usher Syndrome by Jodi Cutler Del Dottore Patient ExpertHealth Maven he said it is available for download but I can't find it anywhere.) It's specific for deafness inherited in a dominant... Loss . These piggy-backed on a 3-day scientific conference, Molecular Biology of Hearing and Deafness...
Genetics Home Reference: dopa-responsive dystonia by nih.gov , it can have either an autosomal recessive or, less commonly, an autosomal dominant pattern of inheritance...  ; autosomal  ; autosomal dominant  ; autosomal recessive  ; bradykinesia  ; cell  ; clubfoot...
Genetics Home Reference: familial erythrocytosis by nih.gov  ; autosomal  ; autosomal dominant  ; autosomal recessive  ; benign  ; bone marrow  ; cell  ; chronic.... When the condition is caused by mutations in the EPOR, EGLN1, or EPAS1 gene, it has an autosomal dominant pattern...
Trying to Understand by Drew's Dad . Patient Expert of X-linked conditions are X-linked recessive, meaning that one normal (working) copy of the gene would compensate for a non-working copy. It is much more common for males to have X-linked recessive conditions...

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Causes ... nt ways. These are described below. Autosomal dominant Autosomal dominant inheritance of CMT ... » Read on
Introduction ... of the condition. This is sometimes called non-inherited or non-hereditary PKD. About 10% of cases of ADPKD ar ... » Read on