Cockayne syndrome
An autosomal recessive syndrome caused by mutations in the ERCC8 and ERCC6 genes. It is characterized by growth and developmental delay, vision and hearing impairment, and impairment of the peripheral nervous system function.
Recent Cases of Cockayne syndrome
Browse recently discussed Cockayne syndrome cases by specialists
Cri du chat. It means cry of a cat in french
Top Cockayne syndrome Doctors on Curofy
Top doctors who continously share their opinions on Cockayne syndrome
Zonal Hospital. Dharamshala
Radiologist
Igmc Shimla
DMRD
Eye Care & Research Centre, Kolkata for About 25 Years
Consultant
Eye Care & Research Centre, Kolkata
MS, DO
JLNM RAINAWARI
Consultant Pediatrics
GMC SRINAGAR
MD Pediatrics
Mirik BPHC
Worked at Mirik B.PH.C As a B.M.OH
North Nengal Medical Collage
M.B.B.S
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