This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Investigations in suspected FRDA

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

investigations

Aim of primary care investigations carried out on FRDA patients is to exclude medical and neurological conditions that may contribute to ataxia. Diagnostic investigations in adults include:

  • U&Es
  • creatinine
  • FBC,
  • ESR/CRP
  • liver enzymes
  • vitamin B12
  • CXR

Secondary care investigations are generally done by a neurologist, with referral and input from other specialists as appropriate e.g – MRI brain and cervical spine, coeliac screen, caerulopasmin/copper etc.

Genetic tests should be considered for common inherited ataxias, particularly if there is a family history.

A child who presents with ataxic symptoms should be referred urgently to the local paediatric services (1).

Reference:


Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.