Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene

Keyphrases

• Early Presentation 100%
• Vocal Cord Paralysis 100%
• SEPT9 Gene 100%
• Hereditary Neuralgic Amyotrophy 100%
• Adulthood 25%
• Age of Onset 25%
• Neonate 25%
• Differential Diagnosis 25%
• Three-generation 25%
• Phenotypic Spectrum 25%
• Recurrent Episodes 25%
• Point mutation 25%
• Intubation 25%
• Prolonged Mechanical Ventilation 25%
• Nerve 25%
• Autosomal Dominant Disorder 25%
• Neonatal Period 25%
• Respiratory Distress 25%
• Neonatal Presentation 25%
• SEPT9 25%
• Brachial Plexus Neuropathies 25%

Medicine and Dentistry

• Vocal Cord Paresis 100%
• Hereditary Neuralgic Amyotrophy 100%
• Infancy 25%
• Respiratory Distress 25%
• Differential Diagnosis 25%
• Point Mutation 25%
• Neonate 25%
• Onset Age 25%
• Intubation 25%
• Autosomal Dominant Disorder 25%
• Newborn Period 25%
• Brachial Plexus Neuropathy 25%