Extremely Early Onset Transthyretin Familial Amyloid Polyneuropathy with a Leu55Pro Mutation: A Pediatric Case Report and Literature Review

Medicine and Dentistry

• Pediatrics 100%
• Familial Amyloid Neuropathy 100%
• Transthyretin 100%
• Hypertrophic Cardiomyopathy 66%
• Neuropathy 66%
• Amyloid Protein 66%
• Diseases 66%
• Myocardial Disease 66%
• Gait 33%
• Sensation 33%
• Genetic Analysis 33%
• Endocardium 33%
• Family History 33%
• Subcutaneous Fat 33%
• Nausea and Vomiting 33%
• Gastrointestinal Distress 33%
• Diarrhea 33%
• Autonomic Dysfunction 33%
• Ecchymosis 33%
• Constipation 33%
• Biopsy Technique 33%
• Lower Limb 33%
• Autosomal Dominant Inheritance 33%
• Anhidrosis 33%
• Autonomic Neuropathy 33%
• Orthostatic Intolerance 33%
• Limb Weakness 33%
• Tafamidis 33%
• Stabilizing Agent 33%
• Sensorimotor Neuropathy 33%
• Fat Tissue 33%