Photosensitivity with growth failure and progressive neurodegeneration.
- Specialty
- Dermatology
- Subspecialty
- Dermatology / DNA repair disorders
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, onset in early childhood
- Gene(s) involved
- ERCC2, ERCC3, ERCC6, ERCC8, XPG
- Alternative names & eponyms
- Neill–Dingwall syndrome
Etiology & mechanism
Defective transcription-coupled DNA repair.
Gene(s) involved (5)
Symptoms & signs (8)
In plain terms, someone with Cockayne syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
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Shares symptoms with
2 shared
Chanarin–Dorfman syndrome
developmental delay, hearing loss
2 shared
Cornelia de Lange syndrome
growth failure, hearing loss
2 shared
Fetal hydantoin syndrome
developmental delay, microcephaly
2 shared
Galloway–Mowat syndrome
developmental delay, microcephaly
2 shared
Glucose transporter type 1 deficiency syndrome
developmental delay, microcephaly
2 shared
Hoyeraal–Hreidarsson syndrome
developmental delay, microcephaly
2 shared
Sanjad–Sakati syndrome
growth failure, microcephaly
1 shared
Aicardi syndrome
developmental delay
1 shared
Aicardi–Goutières syndrome
microcephaly
1 shared
Alport syndrome with diffuse leiomyomatosis
hearing loss
Shares genes with
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