
Inborn analgesia (IA) is described in 3 members of a family: a 14 month-old girl, hel father and grandfather on the paternal line. Generalized indifference to pain and visceral analgesia with other senses intact was noted in all patients since birth. Profound reflexes, intellectual development, karyotype, motor and sensory nervous excitation propagation velocities, somatosensory evoked potentials were all normal. Notedly, the IA inheritance was found to be autosome-dominant in this family.
Adult, Chromosome Aberrations, Male, Pain Insensitivity, Congenital, Humans, Infant, Chromosome Disorders, Female, Genes, Dominant
Adult, Chromosome Aberrations, Male, Pain Insensitivity, Congenital, Humans, Infant, Chromosome Disorders, Female, Genes, Dominant
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