Congenital stridor with feeding difficulty as a presenting symptom of Dok7 congenital myasthenic syndrome.
OBJECTIVE: The congenital myasthenic syndromes (CMS) are a group of genetic disorders of neuromuscular transmission causing fatigable weakness. Symptoms may be present from birth, but diagnosis is often delayed for several years, notably in post-synaptic CMS due to mutations in the DOK7 gene. Recent...
Egile Nagusiak: | Jephson, C, Mills, N, Pitt, M, Beeson, D, Aloysius, A, Muntoni, F, Robb, SA, Bailey, C |
---|---|
Formatua: | Journal article |
Hizkuntza: | English |
Argitaratua: |
2010
|
Antzeko izenburuak
-
Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7.
nork: Lashley, D, et al.
Argitaratua: (2010) -
DOK7 congenital myasthenic syndrome in childhood: early diagnostic clues in 23 children.
nork: Klein, A, et al.
Argitaratua: (2013) -
DOK7 congenital myasthenic syndrome in childhood: Early diagnostic clues in 23 children
nork: Klein, A, et al.
Argitaratua: (2013) -
Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations.
nork: Burke, G, et al.
Argitaratua: (2013) -
DOK7 congenital myasthenic syndrome.
nork: Palace, J
Argitaratua: (2012)