English survey

Survey: Narcolepsy and Fraser syndrome

This page is the English version of the voluntary narcolepsy and Fraser syndrome survey. German version

Citizen science · voluntary survey

Narcolepsy and Fraser syndrome: are there overlaps?

This survey collects observations from people with narcolepsy, families with Fraser syndrome, or both. The aim is a first structured overview of possible shared patterns in sleep symptoms, genetics, comorbidities and family history.

This survey is not a clinical study and does not replace medical advice. Please do not enter names of affected children or other family members.

Which situation applies to you?
Basic information
Narcolepsy and genetic tests

Narcolepsy status

Type

Was HLA typing performed?

HLA-DQB1*06:02 result, if known

Was chromosome analysis / karyotyping performed?

Karyotype result, if known

Fraser genetics and sleep symptoms

Relationship to Fraser syndrome

Which gene is affected, if known?

Excessive daytime sleepiness

Sudden loss of muscle tone / cataplexy

Sleep paralysis

Hallucinations when falling asleep or waking

Findings during pregnancy or in the child

Comorbidities and symptoms

Neurology / sleep

Immune system / inflammation

Findings relevant to Fraser syndrome

Reproduction / other

Medication for narcolepsy or daytime sleepiness

Pitolisant (Wakix)

Modafinil

Methylphenidate (Ritalin)

Lisdexamfetamine

Solriamfetol (Sunosi)

Xyrem / Xywav

Venlafaxine

Atomoxetine

Other medication

Family history and contact

Other narcolepsy cases in the family?

Autoimmune diseases in the family?

Cancer, especially stomach / bowel in the family?

Miscarriages in the family?

Kidney problems in the family?

Eye problems in the family?

Sleep disorders in the family?

May we contact you for follow-up questions?

No direct contact details are stored if you leave this field empty.
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