síndrome de Cockayne

Also known as Neill-Dingwall syndrome, Kenny Syndrome, Neill-Dingwall syndrome, Cockayne's syndrome, Hutchinson–Gilford progeria syndrome, HGPS

rare and fatal autosomal recessive neurodegenerative disorder

Research

1,661 papers

Xeroderma pigmentosum-Cockayne syndrome complex.Orphanet journal of rare diseases · 2017
[Cockayne Syndrome].Brain and nerve = Shinkei kenkyu no shinpo · 2019
Insights Into Cockayne Syndrome Type B: What Underlies Its Pathogenesis?Aging cell · 2025
Cockayne Syndrome Linked to Elevated R-Loops Induced by Stalled RNA Polymerase II during Transcription Elongation.Nature communications · 2024
Cockayne Syndrome Group B (CSB): The Regulatory Framework Governing the Multifunctional Protein and Its Plausible Role in Cancer.Cells · 2021

via PubMed

Wikidata facts

Image: 3-patients-with-cockayne-syndrome.webp

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Article · Português

A síndrome de Cockayne é uma doença hereditária rara. Os pacientes afectados têm um excesso de sensibilidade à luz solar, têm estatura reduzida e sofrem de envelhecimento prematuro. O nome da síndrome advém do médico do Reino Unido chamado Edward Alfred Cockayne (1880 - 1956), primeiro a descrevê-la.

Abstract from DBpedia / Wikipedia · CC BY-SA