2015
DOI: 10.1016/j.ijporl.2014.12.009
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Familial congenital bilateral vocal fold paralysis: A novel gene translocation

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Cited by 27 publications
(4 citation statements)
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“…Sixty-seven valid studies were identified. 3,4,10,14-77 A full list of these studies and their characteristics are recorded in Supplemental Tables S1 and S2 (available online). An overview of our methodology is described in Figure 1 .…”
Section: Resultsmentioning
confidence: 99%
“…Sixty-seven valid studies were identified. 3,4,10,14-77 A full list of these studies and their characteristics are recorded in Supplemental Tables S1 and S2 (available online). An overview of our methodology is described in Figure 1 .…”
Section: Resultsmentioning
confidence: 99%
“…Williams syndrome, Moebius syndrome, congenital myasthenic syndrome, 22q deletion syndrome, and Down syndrome have occasionally been associated with BVCP in the neonatal period. Small series of familial congenital BVCP with variable inheritance patterns and chromosomal alterations have also been described [ 16 ].…”
Section: Discussionmentioning
confidence: 99%
“…Bei vorsichtigem Vorgehen können auch die IA-Muskeln weitgehend geschont werden. Aus Langzeitbeobachtungen ist bekannt, dass angeborene beidseitige Stimmlippenmotilitätsstörungen, deren Ätiologie 138 139 und Zuordnung zu einer Schädigung des ersten oder zweiten Motoneurons noch unklar sind, sich noch bis zum 10. Lebensjahr erholen können 140 141 .…”
Section: Beidseitige Stimmlippenlähmungunclassified