It is feasible that the primary title of the report Cockayne Syndrome is not the name you expected. Kindly inspect the basic synonyms providing to find the alternative name(s) as well as disorder neighborhood(s) covered by this report.
- Deafness-Dwarfism-Retinal Degeneration
- Dwarfism with Renal Degeneration as well as Deafness
- Neill-Dingwall Disorder
- Progeroid Nanism
- Classical Kind, Cockayne Disorder Kind I (Kind A)
- Genetic Kind, Cockayne Syndrome Kind II (Type B)
- Late Beginning, Cockayne Disorder Type III (Kind C)
Cockayne Syndrome (CS) is an unusual form of dwarfism. It is an inherited disorder whose medical diagnosis relies on the presence of 3 indications (1) development retardation, i.e. brief stature, (2) abnormal sensitivity to light (photosensitivity), and also (3) prematurely aged appearance (progeria). In the classic form of Cockayne Disorder (CS type I) the symptoms are progressive and usually emerge after the age of one year. A very early beginning or hereditary type of Cockayne Syndrome (CS kind II) appears at birth (hereditary). There is a 3rd kind, known as Cockayne Disorder Kind III (CS kind III), that provides later in the kid’s growth and also is typically a milder kind of the condition. A 4th form; currently recognized as Xeroderma pigmentosa-Cockayne syndrome (XP-CS), combines features of both of these problems.