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Familial infantile myasthenia.
Robertson WC, Chun RW, Kornguth SE. Robertson WC, et al. Arch Neurol. 1980 Feb;37(2):117-9. doi: 10.1001/archneur.1980.00500510075018. Arch Neurol. 1980. PMID: 6243929
Familial infantile myasthenia is a rare type of myasthenia that usually occurs in connection with respiratory depression. ...Since the condition responds to anticholinesterase medication, early diagnosis is important. Familial infantile myast …
Familial infantile myasthenia is a rare type of myasthenia that usually occurs in connection with respiratory depressio …
Familial infantile myasthenia gravis. Report of three cases with follow-up until adult life.
Gieron MA, Korthals JK. Gieron MA, et al. Arch Neurol. 1985 Feb;42(2):143-4. doi: 10.1001/archneur.1985.04060020053015. Arch Neurol. 1985. PMID: 3977641
We describe three siblings with familial infantile myasthenia gravis (FIMG). Contrary to previous reports suggesting a benign course of FIMG beyond the infantile period, our two patients had severe respiratory exacerbations in early adult life. ...
We describe three siblings with familial infantile myasthenia gravis (FIMG). Contrary to previous reports suggesting a …
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes.
Menold MM, Sadeh M, Lennon F, Blatt I, Goldhammer Y, Yamaoka LH, Vance JM, Pericak-Vance MA. Menold MM, et al. Hum Hered. 1998 Nov-Dec;48(6):325-32. doi: 10.1159/000022824. Hum Hered. 1998. PMID: 9813454
The cause of many cases of CMS has been traced to mutations in the genes for the acetylcholine receptor (AChR) subunits, previously mapped to chromosomes 2 and 17. Recently, an additional form of CMS known as familial infantile myasthenia (FIM) was linked to …
The cause of many cases of CMS has been traced to mutations in the genes for the acetylcholine receptor (AChR) subunits, previously mapped t …