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Brainstem dysfunction in variegate porphyria
被引:5
|作者:
Barraza, Gonzalo
[1
]
Serranova, Tereza
[1
]
Herrero, Carmen
[2
,3
]
Casanova-molla, Jordi
[1
]
To-figueras, Jordi
[2
,3
]
Herranz, Javier
[4
]
Valls-sole, Josep
[1
]
机构:
[1] Hosp Clin Barcelona, Dept Neurol, EMG & Motor Control Unit, E-08036 Barcelona, Spain
[2] Hosp Clin Barcelona, Dept Dermatol, E-08036 Barcelona, Spain
[3] Hosp Clin Barcelona, Biochem & Mol Dept, Porphyria Unit, E-08036 Barcelona, Spain
[4] Hosp Gen Cataluna, Dept Internal Med, Barcelona, Spain
关键词:
acute porphyrias;
axonal polyneuropathy;
brainstem reflexes;
metabolic disorder;
variegate porphyria;
CENTRAL PONTINE MYELINOLYSIS;
ACUTE INTERMITTENT PORPHYRIA;
ANTIDIURETIC-HORMONE;
EXTRAPONTINE MYELINOLYSIS;
TRIGEMINAL NERVE;
DIAGNOSIS;
REFLEX;
DISORDERS;
MUSCLE;
D O I:
10.1002/mus.23367
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Introduction: Variegate porphyria (VP) is a rare metabolic disorder that may present as an acute predominantly motor neuropathy. Cranial nerves and brainstem functions have been only scarcely studied. Methods: Brainstem reflexes were examined in symptomatic and non-symptomatic VP mutation carriers of a single family. Results: Similar results were found in the 2 patients with a history of porphyric crises. The blink reflex showed an absence of late responses (R2 and R2c) to stimulation of both sides. The masseter inhibitory reflex showed reduced inhibition of the second phase. The jaw jerk was normal. The asymptomatic carriers did not show any of the abnormalities just noted. Conclusions: Our results are compatible with a central lower ponsupper medulla disorder in the brainstem. We hypothesize that brainstem dysfunction in VP patients with a history of porphyric crises may be due to neurotoxic effects of porphyrin precursors as well as subclinical osmolarity changes due to hyponatremia. Muscle Nerve 46: 426433, 2012
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页码:426 / 433
页数:8
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