Catalog
Cockayne syndrome
No MMS code
Link to WHO Definition
Cockayne syndrome – http://id.who.int/icd/entity/1206275070
Cockayne syndrome (CS) is a multisystem condition characterised by short stature, a characteristic facial appearance, premature aging, photosensitivity, progressive neurological dysfunction, and intellectual deficit. The annual incidence of CS is close to 1/200,000 in European countries. Disease severity and the age of onset are variable. In classical type I CS, the first symptoms usually appear during the first year of life. Early-onset cases with more severe symptoms (type II) and late-onset cases with milder symptoms (type III) have also been described. CS belongs to the family of NER (nucleotide excision repair)-related disorders.
Parents
- EC10 Genetic syndromes with poikiloderma
- LD2B Syndromes with premature ageing appearance as a major feature
- DNA instability syndromes affecting the skin
- LD2H Syndromic genetic deafness
- Inherited cancer-predisposing syndromes
- Syndromic conditions with disorders of intellectual development as a relevant clinical feature