Cockayne syndrome (CS) is a rare autosomal genetic disorder characterized by types or a spectrum of symptoms such as poor growth, skeletal anomalies, premature aging, and others. Symptoms may ...

Cockayne syndrome is a rare disease, which occurs in about 1 in 500,000 babies. Aesthetically the babies’ symptoms include smaller-than-usual heads, growth deficiencies, sunken eyes and looking ...

Cockayne syndrome (CS) is very rare disease resulting in slow growth in babies as well as rapid aging (a form of progeria). Persons with this syndrome have smaller than normal head sizes ...

Cockayne syndrome is a severe autosomal recessive disorder caused by defective DNA repair mechanisms. People with the disease have much reduced life expectancy and suffer from facial deformities ...

Cockayne syndrome (CS) is very rare disease resulting in slow growth in babies as well as rapid aging (a form of progeria). Persons with this syndrome have smaller than normal head sizes ...

Mainly present in children and young adults, those with Cockayne syndrome often experience significant growth failure, microcephaly, vision and hearing problems, and global developmental delays.

Researchers decode repair mechanism during transcription of genetic information. Cockayne syndrome is a severe autosomal recessive disorder caused by defective DNA repair mechanisms. People with ...