Genes in panel

Adult onset movement disorder

Gene: CYP27A1

Green List (high evidence)

CYP27A1 (cytochrome P450 family 27 subfamily A member 1)
EnsemblGeneIds (GRCh38): ENSG00000135929
EnsemblGeneIds (GRCh37): ENSG00000135929
OMIM: 606530, Gene2Phenotype
CYP27A1 is in 29 panels

3 reviews

Louise Daugherty (Genomics England Curator)

I don't know

Review and rating from Emily Jones (North Bristol NHS Trust) on behalf of South West GLH for GMS Neurology specialist test group.
Created: 23 Apr 2019, 12:18 p.m.

Emily Jones (North Bristol NHS Trust)

Green List (high evidence)

Dystonia is not listed on OMIM as feature of CTX, but GeneReviews for this disorder (adult onset) does include dystonia. On PMID 24442603 ataxia is listed on suspicion index
Created: 23 Apr 2019, 12:14 p.m.

Phenotypes
Cerebrotendinous xanthomatosis, CTX, 213700

Publications

Philip Dawson (Leadiant Biosciences)

Green List (high evidence)

1. In 2018, Stelten et al published a literature review ‘Movement Disorders in cerebrotendinous xanthomatosis’ in which they presented 55 CTX patients with a movement disorder from 39 articles and 7 patients with Parkinsonism from a cohort of 79 Dutch CTX patients. 1
A movement disorder was the presenting symptom in 18% of cases.
However, they also state that ‘Unusual movement disorders represent a rare clinical feature in CTX, but CTX should be considered in the differential diagnosis of these movement disorders, particularly in case of early onset, and when associated with other neurological features (especially cognitive impairment, pyramidal and cerebellar signs) and/or with systemic features (such as diarrhoea, cataract and tendon xanthomas).’
2. Also in 2018, Wong et al published the results of another literature review which identified 91 publications and 194 cases which was presented along with their own case series of 5 patient. This quote from the results section shows that CTX can cause corticospinal tract abnormalities, ataxia, gait difficulties and parkinsonism. 2
‘Of these 194 CTX patients, 116 (59.8%) had CST abnormalities, 114 (58.8%) had ataxia, 90 (46.4%) had cognitive decline, 74 (38.1%) had gait difficulty, 41 (21.1%) had sensory loss, 37 (19.1%) had seizure, 36 (18.6%) had speech changes, 34 (17.5%) had psychiatric changes, and 19 (9.8%) had parkinsonism;68 (35.0%) had baseline cognitive problems.’
They also calculated Cumulative Incidence Function (CIF) for each CTX symptom which gives an indication of the likelihood of a particular symptom having developed at any given age (best- & worst-case scenario) based on a subset of cases where age of symptom onset was available. The CIF graphs show that whilst Parkinsonism is unlikely to develop before the age of 20, symptoms of ataxia, corticospinal tract abnormalities and gait difficulties can develop in both childhood or adulthood with increasing incidence with age.
References
1. Stelten et al, Movement disorders in cerebrotendinous Xanthomatosis. Park Rel Dis. 2018; 07.006
2. Wong et al, Natural history of neurological abnormalities in cerebrotendinous xanthomatosis. J Inherit Metab Dis. 2018 Jul;41(4):647-656
Created: 18 Apr 2019, 3:20 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Cerebrotendinous xanthomatosis, 213700; Dystonia, including childhood & adult onset.

Publications

History Filter Activity

27 Apr 2019, Gel status: 3

Set mode of inheritance

Louise Daugherty (Genomics England Curator)

Mode of inheritance for gene: CYP27A1 was changed from to BIALLELIC, autosomal or pseudoautosomal

27 Apr 2019, Gel status: 3

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for gene: CYP27A1 were changed from Cerebrotendinous xanthomatosis, CTX, 213700; Dystonia to Cerebrotendinous xanthomatosis, CTX, 213700; Dystonia; Dystonia, including childhood & adult onset

27 Apr 2019, Gel status: 3

Set publications

Louise Daugherty (Genomics England Curator)

Publications for gene: CYP27A1 were set to 24442603

27 Apr 2019, Gel status: 3

Entity classified by Genomics England curator

Louise Daugherty (Genomics England Curator)

Gene: cyp27a1 has been classified as Green List (High Evidence).

23 Apr 2019, Gel status: 1

Set Phenotypes, Set publications

Louise Daugherty (Genomics England Curator)

Added phenotypes Cerebrotendinous xanthomatosis, CTX, 213700 for gene: CYP27A1 Publications for gene CYP27A1 were changed from to 24442603

23 Apr 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source NHS GMS was added to CYP27A1.

23 Apr 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source South West GLH was added to CYP27A1.

3 Jan 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: CYP27A1 was added gene: CYP27A1 was added to Adult onset movement disorder. Sources: Expert Review Red Mode of inheritance for gene: CYP27A1 was set to Phenotypes for gene: CYP27A1 were set to Dystonia