<p>The
Myotubular and Centronuclear Myopathy Patient Registry (‘MTM and CNM Registry’)
is an international database specific to these conditions, operated by
Newcastle University in the UK as part of the global TREAT-NMD Neuromuscular
Network. The registry was developed in partnership with the MTM and CNM
communities and is jointly funded by the Myotubular Trust, Muscular Dystrophy
UK, and Audentes Therapeutics. </p><p><br></p>
<p>Participants
register online and must provide consent before accessing the registry
questionnaire. The clinical data are provided by the participants, and the
genetic data are obtained by the Registry Curator via the genetic report.</p>
<p><br></p>
<p>The
MTM & CNM Registry aims to:</p><p><br></p>
<ul>
<li>Help identify patients for relevant clinical trials as they become
available.</li>
<li>Encourage further research into myotubular and centronuclear
myopathy.</li>
<li>Provide researchers with specific patient information to support
their research.</li>
<li>Assist doctors and other health professionals by providing them
with up-to-date information on managing myotubular and centronuclear
myopathy, to help them deliver better standards of care for their
patients.</li></ul><div><br></div>
<p>The
investigators welcome the registration of:</p><p><br></p>
<ul>
<li>All patients with a myotubular myopathy or centronuclear myopathy
diagnosis, which has been confirmed via genetic testing or muscle biopsy.</li>
<li>Any carrier females of x-linked myotubular myopathy, especially if
they have manifested myotubular myopathy type symptoms.</li>
<li>Any patient who is deceased, but who had a confirmed diagnosis.</li>
</ul>
<p><b> </b></p>
<p>The
registry dataset includes patient reported clinical diagnosis, genetic
mutation, motor function, wheelchair use, respiratory function, ventilation
type, chest infection, feeding and heart function, neuromuscular examinations,
scoliosis surgery, family history and other registries joined. Patient genetic
report and muscle biopsy report are also uploaded to the registry if available,
with details of clinician and where the tests were conducted.</p>