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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Cockayne Syndrome | Legal notice |
Other terms
Syndrome, Cockayne,Progeria-Like Syndrome,Progeria Like Syndrome,Progeria-Like Syndromes,Syndrome, Progeria-Like,Cockayne Syndrome, Type III,Cockayne Syndrome Type C,Group C Cockayne Syndrome,Type III Cockayne Syndrome,Cockayne Syndrome, Type C,Cockayne Syndrome, Group C,Cockayne Syndrome Type 3,Type C Cockayne Syndrome,Cockayne Syndrome, Type II,Type II Cockayne Syndrome,Group B Cockayne Syndrome,Type B Cockayne Syndrome,Cockayne Syndrome, Group B,Cockayne Syndrome, Type B,Cockayne Syndrome, Type I,Type I Cockayne Syndrome,Group A Cockayne Syndrome,Type A Cockayne Syndrome,Cockayne Syndrome, Group A,Cockayne Syndrome, Type A
Description
Cockayne Syndrome: A 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 recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.
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- Dwarfism
- Heredodegenerative Disorders, Nervous System
- Abnormalities, Multiple
- Dwarfism
- Heredodegenerative Disorders, Nervous System
Legal notice
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The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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