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Familial insensitivity to pain (HSAN V) and a mutation in the NGFB gene. A neurophysiological and pathological study.
Umeå University, Faculty of Medicine, Surgical and Perioperative Sciences, Orthopaedics.
Umeå University, Faculty of Medicine, Surgical and Perioperative Sciences, Orthopaedics.
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2004 (English)In: Muscle and Nerve, ISSN 0148-639X, Vol. 30, no 6, 752-760 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 30, no 6, 752-760 p.
Keyword [en]
Adult, Aged, Aged; 80 and over, Child, Female, Hereditary Sensory and Autonomic Neuropathies/*genetics/*physiopathology/radiography, Humans, Male, Mutation, Nerve Growth Factor/*genetics, Pedigree, Sural Nerve/pathology
URN: urn:nbn:se:umu:diva-14113DOI: 10.1002/mus.20172PubMedID: 15468048OAI: diva2:153784
Available from: 2007-05-23 Created: 2007-05-23 Last updated: 2009-10-12Bibliographically approved
In thesis
1. Norrbottnian congenital insensitivity to pain
Open this publication in new window or tab >>Norrbottnian congenital insensitivity to pain
2006 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Congenital insensitivity to pain is a rare hereditary neuropathy. We present patients from a large family in Norrbotten, Sweden with a mutation in the nerve growth factor β gene (NGFß). Using a model of recessive inheritance, we identified an 8.3-Mb region on chromosome 1p11.2-p13.2 shared by the affected individuals in the family. Analysis of candidate genes in the disease-critical region revealed a mutation in the coding region of the NGFß gene specific for the disease haplotype. All three severely affected individuals were homozygous for the mutation. The disease haplotype was also observed in both unaffected and mildly affected family members, but in heterozygote form. We have identified 43 patients, 3 homozygous and 40 heterozygous. The homozygous patients have a severe congenital form with onset of symptoms at an early age, most often affecting the lower extremities with insidious progressive joint swellings or painless fractures. Fracture healing was normal, but the arthropathy was progressive, resulting in disabling Charcot joints with gross deformity and instability. These patients lacked deep pain perception in bones and joints and had no protective reflexes, leading to gross bone and joint complications. They also had abnormal temperature perception but normal ability to sweat. There was no mental retardation. Clinically, they fit best into the group HSAN type V. Sural nerve biopsies showed a moderate loss of thin myelinated fibers (Ad-fibers) and a severe reduction of unmyelinated fibers (C-fibers). 14 of the 40 heterozygous adult patients had mild or moderate problems with joint deformities, usually with only slight discomfort. Treatment was conservative with (if needed) different kinds of orthosis and in some cases joint replacement. Three patients had only neuropathy, and 16 patients had no symptoms.

In congenital disorders like these, it is important to evaluate the age and also the slowly progressive nature, when considering treatment. There is an increased risk of growth disturbances in the very young. The orthopedic operations should therefore be planned from a long-term point of view, but patient education and orthosis are cornerstones in the treatment—to delay the development of neuropathic arthropathy. Arthrodesis, limb lengthening and spinal decompression with fusions are the only elective procedures that seem reasonable.

This Norrbottnian disease is also interesting as a model system for the study of pain.

Place, publisher, year, edition, pages
Umeå: Kirurgisk och perioperativ vetenskap, 2006. 32 p.
Umeå University medical dissertations, ISSN 0346-6612 ; 1020
Pain insensitivity, HSAN
National Category
urn:nbn:se:umu:diva-746 (URN)91-7264-057-X (ISBN)
Public defence
2006-04-28, Betula, 6M, Norrlands universitetssjukhus, Umeå, 09:00 (English)
Available from: 2006-04-07 Created: 2006-04-07 Last updated: 2010-01-18Bibliographically approved

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