1Dyck PJ,Mellinger JF,Reagan TJ,et al. Not indifference to pain but varieties of hereditary sensory and autonomic neuropathy. Brain, 1953,106:373
2Hilz MJ. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiolugical examinations. Clin Auton Res ,2002,12 : 133
3Verpoorten N, Claeys KG, Deprez L, et al. Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene ( NTRK1 ) associated with hereditary sensory neuropathy type Ⅳ. Neuromuscul Disord ,2006,16 : 19
5Schulman H,Tsodikow V, Einhorn M, et al. Congenital insensitivity to pain with anhidrosis ( CIPA ) : the spectrum of radiological findings. Pediatr Radiol,2001,31:701
2Asaumi K, Nakanishi T, Asahara H, et al. Expression of neurotrophins and their receptors (Trk) during fracture healing[J]. Bone,2000,26(6): 625~33.
3Bodzioch M, Lapicka K, Aslanidis C, et al. Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice mutation in intron 5 and cluster of four mutations in exon 15[J]. Hum Mutat, 2001,17(1):72.
4Bonkowsky JL, Johnson J, Carey JC, et al. An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis[J]. Pediatrics,2003,112(3 Pt 1): 237~41.
5Shorer Z, Moses SW, Hershkovitz E, et al. Neurophysiologic studies in congenital insensitivity to pain with anhidrosis[J]. Pediatr Neurol,2001,25(5):397~400.