DOK7 congenital myasthenic syndrome in childhood: Early diagnostic clues in 23 children
Mutations in DOK7 are a common cause of congenital myasthenia. Treatment with ephedrine or salbutamol is effective, but diagnosis is often delayed. The aim of our study was to find early clues to the diagnosis of DOK7 congenital myasthenic syndrome. We included 23 children of 20 families. Onset of s...
Հիմնական հեղինակներ: | Klein, A, Pitt, M, McHugh, J, Niks, E, Sewry, C, Phadke, R, Feng, L, Manzur, A, Tirupathi, S, DeVile, C, Jayawant, S, Finlayson, S, Palace, J, Muntoni, F, Beeson, D, Robb, SA |
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Ձևաչափ: | Journal article |
Լեզու: | English |
Հրապարակվել է: |
2013
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Նմանատիպ նյութեր
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DOK7 congenital myasthenic syndrome in childhood: early diagnostic clues in 23 children.
: Klein, A, և այլն
Հրապարակվել է: (2013) -
Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations.
: Burke, G, և այլն
Հրապարակվել է: (2013) -
Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7.
: Lashley, D, և այլն
Հրապարակվել է: (2010) -
Congenital stridor with feeding difficulty as a presenting symptom of Dok7 congenital myasthenic syndrome.
: Jephson, C, և այլն
Հրապարակվել է: (2010) -
DOK7 congenital myasthenic syndrome.
: Palace, J
Հրապարակվել է: (2012)