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Cockayne syndrome

MONDO:0016006

A multisystem condition characterized by short stature, a characteristic facial appearance, premature aging, photosensitivity, progressive neurological dysfunction, and intellectual deficit.

Also known as: dwarfism-retinal atrophy-deafness syndrome, progeria-like syndrome, progeroid nanism

36 clinical trials for this condition and its sub-types.

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Sub-types

Cockayne spectrum with or without cerebrooculofacioskeletal syndrome (0) Cockayne syndrome type 1 (0) Cockayne syndrome type 2 (0) Cockayne syndrome type 3 (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inborn errors of metabolism (42) Human disease (14) DNA repair disease (11) Developmental defect during embryogenesis (7) Premature aging syndrome (6) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2)

Trials to join now! 18 Not yet recruiting 3 Not yet finished but already full! 5 Completed 10

Cockayne syndrome

Sub-types

Broader categories

New combo therapy targets cancer's DNA repair weakness

New vitamin supplements aim to make life easier for kids with rare metabolic disorders

New program aims to ease burden on families of kids with rare diseases

Massive genetic study aims to unlock secrets of rare metabolic diseases

Study on COVID-19 and metabolic disorders pulled before it began