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:: How to recognise Neurocanthocytosis

The first signs of the diseases in the neuroacanthocytosis (NA) group are subtle and easily overlooked. Initial symptoms, which often occur in the person’s mid 20’s, may include grunts or tic noises made unconsciously in the throat, progressing to drooling and problems in controlling the tongue from ejecting food. Involuntary biting of the tongue, lips and/or cheeks may follow.

At the beginning there can be a general, slight physical awkwardness. Things on a shelf are knocked off for no apparent reason. Difficulty with walking and balance can also be early symptoms. Problems controlling trunk, leg and arm movements are often barely noticeable at the beginning, but become increasingly difficult as the disease progresses. Several patients find it difficult to sleep at night and others report fatigue and weakness.

Personality change may also be an early indication. The carefree young adult becomes obsessive-compulsive and uncharacteristically forgetful or just loses confidence or drive. Fainting or epileptic seizures may also occur. Mood changes may happen and a person often becomes isolated, in part out of embarrassment.

There are several reports of the problems beginning after a traumatic event including physical attack, unexpected failure of an exam and birth of a child.

CLINICAL SIGNS

A defining symptom that is not apparent is the spiky red blood cells, or acanthocytes, from which the NA disease group takes its name. These unusual blood cells can be observed with a microscope in some circumstances. Still more difficult to observe are the alterations or mutations in patients’ genes. Each of the NA group diseases has a different genetic characteristic that can be determined only by blood tests.

A person showing some of this pattern of symptoms should see a neurologist. Clinicians and patients can also visit www.naadvocacy.org for links to further scientific reports. Full details are also available on the free blood testing service offered by the Advocacy for Neuroacanthocytosis Patients, aimed at helping determine a definitive diagnosis for NA.



:: Useful NA Resources

  • Neuroacanthocytosis Syndromes II, published December 2007, the book provides a profound insight into recent developments within the field of neuroacanthocytosis syndromes. Edited by Ruth H. Walker, Shinji Saiki and Adrian Danek. Available at amazon.com
  • A Western blot test for the presence of chorein in the membranes of red blood cells can be offered free of charge due to support of the Advocacy for Neuroacanthocytosis Patients'. Download instructions on the blood sampling and specimen shipment as a PDF or get more information on the method at PubMed
  • The entry for chorea acanthocytosis in GeneReviews is the most complete, readily available report on ChAc. Published by the University of Washington with the support of the National Institutes of Health
  • A dedicated Patient & Families Support Group at Yahoo Groups offers patients and families information, advice, support or just an understanding ear
  • Visit PubMed for access to NA research in English from the Medline database.
  • Search Google for the latest on NA
  • Visit the NA page on WeMove, the Movement Disorder Societies charitable and educational associate



:: naadvocacy.org

naadvocacy.org is the website of the The Institute for Neuroacanthocytosis. It is the Advocacy's international centre for supporting patients and promoting clinical and basic research. The website provides access to resources found on the website.

  • Patients' Centre
  • Clinic
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  • Symposia
  • NA News
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Adrian Danek presents EMINA2 E-Rare Athens

NANews23 - Adrian Danek talk in Rome

In January Adrian Danek attended the 2014 E-Rare Scientific Meeting and Strategic Workshop in Athens and presented a session about EMINA2, the ongoing research work funded under the E-RARE programme of the European Union. EMINA  (European Multidisciplinary Initiative on Neuroacanthocytosis) is now a group of five university laboratories coordinated by Andreas Hermann of the Dresden University of Technology and including Nicola Andrea Grzeschik of University Medical Center Groningen, The Netherlands, Mario Mairhofer of Medical University of Vienna, Austria, Merel Adjobo-Hermans of  Radboud University Nijmegen Medical Centre, The Netherlands and Pablo Blinder of the Neuroscience Department, Tel-Aviv University, Israel.

Dr. Danek described how 6 partners in 5 countries with both clinical and basic science features are working to reach a clearer understanding of the functioning of both normal and abnormal cells in chorea-acanthocytosis patients.  They have a number of approaches to the mysteries of the causes of the NA diseases including using patients' stem cells to study the effects of certain mutations on intracellular signalling pathways. A poster was also displayed.  Working closely with the EMINA2 partners are the "friends of EMINA2" that include Lucia de Franceschi at University of Verona, Antonio Baeza Velayos  at  the Wellcome Centre for Human Genetics, University of Oxford, researchers who are supported by Advocacy research grants as well as Adrian Danek, the founder of the NA movement, at Ludwig Maximilians Universität, Munich .

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