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Neuroacanthocytosis - Clinical variability (a report on six cases)

Dulski, J. (författare)
Soltan, W. (författare)
Schinwelski, M. (författare)
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Sitek, E. J. (författare)
Rudzinska, Monika (författare)
Wójcik-Pedziwiatr, M. (författare)
Wictor, L. (författare)
Lund University,Lunds universitet,Neurologi, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Neurology, Lund,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine
Schön, F. (författare)
Puschmann, A. (författare)
Lund University,Lunds universitet,Neurologi, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Neurology, Lund,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine
Klempir, J. (författare)
Tilley, L. (författare)
Roth, J (författare)
Tacik, P. (författare)
Fujioka, Shinsuke (författare)
Traynor, S. (författare)
Wszolek, Z K (författare)
Drozdowski, W. (författare)
Slawek, Jaroslaw (författare)
visa färre...
 (creator_code:org_t)
John Wiley and Sons Inc. 2014-05-01
Engelska.
Ingår i: Movement Disorders. - : John Wiley and Sons Inc.. - 0885-3185. ; 29:Suppl 1, s. 194-194
  • Konferensbidrag (refereegranskat)
Abstract Ämnesord
Stäng  
  • Objective: To provide clinical clues to differential diagnosis in patients with chorea and other movement disorders with blood acanthocytes. Background: Neuroacanthocytosis (NA) is an umbrella term for neurological conditions associated with acanthocytosis. Core NA syndromes, with basal ganglia involvement and in which acanthocytosis is a frequent finding, include autosomal recessive choreaacanthocytosis (Ch-Ac) and X-linked McLeod syndrome (MLS). Due to the very low prevalence, scarcity of data and high clinical variability they may be underdiagnosed. Methods: Six male patients (pts), three diagnosed with Ch-Ac: 33-y.o.(no.1), 35-y.o.(no.2), 42-y.o.(no.3), two diagnosed with MLS: 52-y.o.(no.4), 60-y.o.(no.5) and one 62-y.o.(no.6), a brother of no.5, with clinical suspicion of MLS. The patients had an unremarkable family history and were asymptomatic until adulthood. Pts no.1,2,4,5,6 developed generalized chorea and patient no.3 had predominant bradykinesia. Pts no.1,2,3 had phonic and motor tics, additionally pts no.1 and 2 exhibited peculiar oromandibular dystonia with tongue thrusting. In pts no.2 and 3 dystonic supination of feet was observed, patient no.3 subsequently developed bilateral foot drop. Pts no. 2 and 4 had signs of muscle atrophy. Tendon reflexes were decreased or absent and electroneurography demonstrated sensorimotor neuropathy in patients no. 1,2,3,4,5, except no. 6. Generalized seizures were seen in patients no.2,3,5,6 and myoclonic jerks in patient no 1. Cognitive deterioration was reported in patients no.1,2,3,5,6. Serum creatine kinase levels were elevated in all six patients. Results: Peripheral blood smears revealed acanthocytosis in patients no.1,2,3,5,6, except no. 4. In patients no. 1 and 3 reduced expression of chorein was detected on Western blot. In patient no. 2 genetic testing showed mutations in VPS13A gene and in no.4 and 5 genetic analysis confirmed mutations in XK gene (MLS). The time from the onset of symptoms till establishing the diagnosis in patients no. 1,2,3,4,5 was 11,5,7,6,32 years respectively. Patient no.4 suddenly developed multiple organ failure and died of cardiac arrhythmia at the age of 52. Conclusions: We highlight the variability of clinical presentation of NA syndromes and the long time from the onset to diagnosis with the need to screen the blood smears in uncertain cases, however, as in one of our cases acanthocytes may even be not found.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Nyckelord

neuroacanthocytosis
motor dysfunction
Parkinson disease
human
patient
acanthocytosis
hospital patient
chorea
blood smear
diagnosis
mutation
blood
gene
basal ganglion
bradykinesia
differential diagnosis
adulthood
Western blotting
genetic screening
genetic analysis
tic
autosomal recessive inheritance
tongue
family history
prevalence
oromandibular dystonia
mental deterioration
tonic clonic seizure
sensorimotor neuropathy
McLeod syndrome
electroneurography
tendon reflex
creatine kinase blood level
muscle atrophy
peroneus nerve paralysis
body posture
multiple organ failure
heart arrhythmia
male

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