About The Medical Condition Cockayne Syndrome, Type I
Find the definition of the medical term Cockayne Syndrome, Type I. Cockayne Syndrome, Type I defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Cockayne Syndrome, Type I
| Cockayne Syndrome, Type I Medical Condition |
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What's The Definition Of The Medical Condition Cockayne Syndrome, Type I?
An inherited syndrome phenotypically characterized by unusual facies (large ears and sunken eyes), growth failure, intellectual deterioration, loss of subcutaneous fat, pigmentary retinal degeneration, neural deafness, dwarfism, photosensitivity, optic atrophy, peripheral neuropathy, and cataracts. Pathologic examination reveals a patchy loss of central myelin and white matter atrophy. Cockayne syndrome may be divided into two or more distinct genetic subtypes. (Menkes, Textbook of Child Neurology, 5th ed, p197)
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