[Congenital insensitivity to pain, anhidrosis and premature loss of baby teeth as a symptoms of rare neuropathy]

MeSH terms

• Disease Progression
• Female
• Finland
• Hereditary Sensory and Autonomic Neuropathies / diagnosis*
• Hereditary Sensory and Autonomic Neuropathies / genetics
• Humans
• Infant
• Mutation
• Pain Insensitivity, Congenital / diagnosis*
• Pain Insensitivity, Congenital / genetics
• Pedigree
• Prognosis
• Receptor Protein-Tyrosine Kinases / genetics*
• Risk Assessment
• Severity of Illness Index