Congenital insensitivity to pain

Journal of Bone and Joint Surgery - Series B

Volumn 84, Issue 2, 2002, Pages 252-257

  Bar On, E ^a   Weigl, D ^a   Parvari, R ^a   Katz, K ^a   Weitz, R ^a   Steinberg, T ^a  

^a SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; DNA; HISTAMINE;

ADULT; ARTICLE; ASPIRATION BIOPSY; AVASCULAR NECROSIS; BACTERIUM CULTURE; BONE DEFORMATION; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL ANALGESIA; CONTROLLED STUDY; DEBRIDEMENT; DECUBITUS; DNA DETERMINATION; EPIPHYSIODESIS; FEMALE; FRACTURE; GENE MUTATION; GROWTH DISORDER; HUMAN; JOINT DISLOCATION; MALE; MENTAL DEFICIENCY; NEUROPATHIC JOINT DISEASE; OSTEOTOMY; PATIENT EDUCATION; PRIORITY JOURNAL; QUANTITATIVE ASSAY; SHOE; SUPERINFECTION; SWEAT TEST; WEIGHT BEARING;

EID: 0036207911     PISSN: 0301620X     EISSN: None     Source Type: Journal    
DOI: 10.1302/0301-620X.84B2.11939     Document Type: Article

References (22)

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5. Orthopaedic aspects of congenital insensitivity to pain
6. Orthopaedic manifestations in congenitally insensate patients
7. Charcot joint disease of the shoulders in a patient who had familial sensory neuropathy with anhidrosis: A case report
8. Unsuccessful surgical treatment of hip dislocation in congenital sensory neuropathy with anhidrosis
9. Nonunion of the ulna in a ten-month-old child who had type-IV hereditary neuropathy: A case report
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11. Congenital insensitivity to pain and its orthopedic implications
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13. Congenital insensitivity to pain with anhidrosis: A case report
14. Congenital familial sensory neuropathy with anhidrosis
15. Recurrent dislocation of the hip in congenital indifference to pain: Case report with arthrographic and operative findings
16. Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV)
17. Congenital insensitivity to pain with anhydrosis
18. Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: Genetic heterogenicity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies
19. Orthopedic manifestations of familial dysautonomia: A review of 136 patients
20. Congenital sensory neuropathies: Diagnostic distinction from familial dysautonomia
21. A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis
22. Congenital insensitivity to pain with anhidrosis: Novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor