Jensen syndrome: Introduction
Jensen syndrome: A rare genetic disorder characterized by degeneration of the optic nerve (causing impaired vision), deafness due to nerve damage and dementia due to calcification of the central nervous system. Death usually results by about the age of 40 with extensive calcification of all parts of the nervous system.
More detailed information about the symptoms,
causes, and treatments of Jensen syndrome is available below.
Symptoms of Jensen syndrome
See full list of 7
symptoms of Jensen syndrome
Home Diagnostic Testing
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Jensen syndrome: Related Patient Stories
Jensen syndrome: Complications
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Causes of Jensen syndrome
- The condition is inherited in a X-linked recessive manner and thus only males present with severe symptoms
- more causes...»
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Disease Topics Related To Jensen syndrome
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Jensen syndrome: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Jensen syndrome
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency
is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis).
See symptoms...read more »
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Jensen syndrome: Research Doctors & Specialists
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- Eye Health Specialists (Ophthalmology):
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Evidence Based Medicine Research for Jensen syndrome
Medical research articles related to Jensen syndrome include:
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Jensen syndrome: Animations
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Prognosis for Jensen syndrome
Prognosis for Jensen syndrome:
The prognosis is poor with reported cases resulting in death at about the age of 40 years. Deafness is present at birth, vision loss starts during adolescence and results in blindness and dementia starts in adulthood.
More about prognosis of Jensen syndrome
Research about Jensen syndrome
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Statistics for Jensen syndrome
Jensen syndrome: Broader Related Topics
Types of Jensen syndrome
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Definitions of Jensen syndrome:
Jensen syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Jensen syndrome, or a subtype of Jensen syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Jensen syndrome as a "rare disease".
Source - Orphanet
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