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Cockayne syndromeA genetic disorder that involves progressive multisystem degeneration and is classified as a segmental premature-aging syndrome. Cockayne syndrome is characterized by dwarfism, prematurely aging, visual problems and deafness, sensitivity to sunlight, and mental retardation. Cockayne syndrome is a transcription- and DNA repair deficiency syndrome. T [..]
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Cockayne syndromeA genetic condition characterized by short stature, premature aging, sensitivity to light, and possibly deafness and mental retardation.
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Cockayne syndromeA genetic condition characterized by short stature, premature aging, sensitivity to light, and possibly deafness and mental retardation.
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Cockayne syndromeA Syndrome characterized by multiple system abnormalities including Dwarfism; Photosensitivity Disorders; Premature Aging; and Hearing Loss. It is caused by Mutations of a number of autosomal Recessiv [..]
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Cockayne syndromeCaused by Mutations of Gene CKN1.
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Cockayne syndromeCaused by Mutations of Gene ERCC6.
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Cockayne syndromeType C is a rare form. Its genetic defect is not clear; appears to be a heterogeneous group. OMIM suggests that Type C should not be used anymore.
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Cockayne syndromeA syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessiv [..]
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Cockayne syndromeA genetic condition characterized by short stature, premature aging, sensitivity to light, and possibly deafness and mental retardation.
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Cockayne syndrome
A rare congenital disorder characterized by growth failure, impaired development of the nervous system, abnormal photosensitivity, and premature aging.
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