DOK7 myasthenic syndrome with subacute adult onset during pregnancy and partial response to fluoxetine.
Neuromuscul Disord
; 28(3): 278-282, 2018 03.
Article
en En
| MEDLINE
| ID: mdl-29395672
ABSTRACT
DOK7 congenital myasthenic syndrome (DOK7-CMS) generally presents early in life and is treated with salbutamol or ephedrine. This report describes an atypical case of a 39-year-old woman who presented with proximal upper limb weakness in the third trimester of pregnancy and was initially diagnosed with seronegative myasthenia gravis. Dramatic clinical worsening under pyridostigmine and further inefficacy of steroids, intravenous human immunoglobulin (IVIG) and plasma exchange (PLEX) led to the presumptive diagnosis of a CMS. Initially, a slow-channel CMS was regarded as more probable due to prominent finger extension weakness. Accordingly, fluoxetine was started and a lengthy improvement was seen. Clinical deterioration occurred after fluoxetine withdrawal, when a c.1124_1127dup homozygous mutation was detected in DOK7 gene. Afterwards, salbutamol was started and the patient became asymptomatic. This case highlights the importance of considering CMS before an adult-onset myasthenic syndrome and suggests a benefit from fluoxetine not previously reported in DOK7-CMS.
Palabras clave
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Fluoxetina
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Debilidad Muscular
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Síndromes Miasténicos Congénitos
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Proteínas Musculares
Límite:
Adult
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Female
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Humans
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Pregnancy
Idioma:
En
Revista:
Neuromuscul Disord
Asunto de la revista:
NEUROLOGIA
Año:
2018
Tipo del documento:
Article