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...
Κύριοι συγγραφείς: | 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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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2013
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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DOK7 congenital myasthenic syndrome in childhood: early diagnostic clues in 23 children.
ανά: Klein, A, κ.ά.
Έκδοση: (2013) -
Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations.
ανά: Burke, G, κ.ά.
Έκδοση: (2013) -
Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7.
ανά: Lashley, D, κ.ά.
Έκδοση: (2010) -
Congenital stridor with feeding difficulty as a presenting symptom of Dok7 congenital myasthenic syndrome.
ανά: Jephson, C, κ.ά.
Έκδοση: (2010) -
DOK7 congenital myasthenic syndrome.
ανά: Palace, J
Έκδοση: (2012)