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Example clinical scenario

A family attends clinic concerned because their three-year-old son’s development is delayed: he sat at eight months, did not walk until 18 months and still cannot run, jump or climb stairs. He has delayed speech, with first words at two years. Pregnancy, early life and family history are all unremarkable.

On examination, he is not dysmorphic, he has prominent calves and uses Gowers’ manoeuvre to stand. Blood test results show raised alanine transaminase levels and creatine kinase (CK) levels.

When to consider genomic testing

  • Genomic testing should be considered if there is a strong clinical suspicion of muscular dystrophy. Clinical features include:
    • elevated CK levels;
    • muscle symptoms (weakness, fatigue, pain);
    • speech delay, motor delay or global developmental delay;
    • frequent falls and/or an unusual gait; and
    • isolated alteration in liver enzymes.
  • In boys presenting with features of Duchenne or Becker muscular dystrophy (the most common forms), dystrophin gene testing should be prioritised.
  • In symptomatic girls, a wider differential should be considered. However, as female carriers of Duchenne muscular dystrophy may manifest symptoms, it is reasonable to first test the dystrophin gene.
  • In individuals where dystrophin gene test results are normal, a wider differential diagnosis should be considered, and muscle biopsy and MRI together with extended genomic testing is indicated. The choice of genomic test will depend on the age of the child, together with the pattern of muscle involvement, associated findings (such as dysmorphic features and brain or eye involvement) and any family history.

What do you need to do?

  • Consult the National Genomic Test Directory. From here you can access the rare and inherited disease eligibility criteria, which provides information about individual tests and their associated eligibility criteria. You can also access a spreadsheet containing details of all available tests.
  • To find out which genes are included on different gene panels, see the NHS Genomic Medicine Service (GMS) Signed Off Panels Resource.
  • Decide which of the panels best suits the needs of your patient or family. For muscular dystrophies, there are a number of available panels, including:
    • R73 Duchenne or Becker muscular dystrophy: Identifies point mutations, deletions and duplications in the dystrophin gene (DMD) if you suspect either Duchenne or Becker muscular dystrophies;
    • R82 Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies: If you suspect limb girdle muscular dystrophy;
    • R74 Facioscapulohumeral muscular dystrophy: If you think your patient may have a diagnosis of facioscapulohumeral muscular dystrophy and a DUX4 contraction has not been excluded;
    • R345 Facioscapulohumeral muscular dystrophy – extended testing: If you strongly suspect facioscapulohumeral muscular dystrophy and a DUX4 contraction has been excluded (this encompasses methylation testing of DUX4, SMCDH1 gene sequencing, and extended testing of the 4q locus to look for complex variants);
    • R72 Myotonic dystrophy type 1: If clinical features are strongly suggestive of myotonic dystrophy;
    • R381 Other rare neuromuscular disorders: To be considered if clinical features are atypical and a broader range of genes are potentially causative (this test includes, whole genome sequencing (WGS) and short tandem repeat testing).
    • R89 Ultra rare and atypical monogenic disorders: To be considered if the presentation is unusual and has a wide differential requiring analysis of more than one non-WGS test. In this situation it may be more efficient to utilise WGS and then analyse the genes from several test indications. The test includes WGS and microarray. You will need to list multiple test codes on the request form indicating the genes/conditions you would like to be analysed.
  • For tests that are undertaken using WGS, including R381 and R89, you will need to:
  • For tests that do not include WGS, including R73, R82, R74, R345, and R72:
    • you can use your local Genomic Laboratory Hub test order and consent (RoD) forms; and
    • parental samples may be needed for interpretation of the child’s result. Parental samples can be taken alongside that of the child, and their DNA stored, or can be requested at a later date if needed.
  • The majority of tests are DNA-based, and an EDTA sample (typically a purple-topped tube) is required. Exceptions include karyotype testing and DNA repair defect testing (for chromosome breakage), which require lithium heparin (typically a green-topped tube).
  • Information about patient eligibility and test indications was correct at the time of writing. When requesting a test, please refer to the National Genomic Test Directory to confirm the right test for your patient.

Resources

For clinicians

References:

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  • Last reviewed: 26/09/2024
  • Next review due: 26/09/2025
  • Authors: Dr Elizabeth Radford
  • Reviewers: Dr Elaine Clark, Dr Amy Frost, Dr Eleanor Hay, Dr Joanna Kennedy