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Clinical manifestations of congenital insensitivity to pain with anhidrosis

dc.contributor.authorSantoya Montes, Yanin Elena
dc.contributor.authorPuentes Rozo, Pedro
dc.date.accessioned2023-07-21T16:27:01Z
dc.date.available2023-07-21T16:27:01Z
dc.date.issued2020
dc.date.submitted2023
dc.identifier.citationSANTOYA MONTES, Y. E., & PUENTES ROZO, P. E. D. R. O. (2020). Clinicai manifestations of congenital Insensitivity to pain with anhidrosis. Revista Salud Uninorte, 36(1), 178-195.spa
dc.identifier.urihttps://hdl.handle.net/20.500.12585/12357
dc.description.abstractIntroduction: The congenital insensitivity to pain with anhidrosis (HSAN IV) is a rare disease, which results in different with multisystem symptoms, impacting cognitive functions that affect negatively the quality of life not only in patients but also in relatives. It is estimated that most individuals suffering from this disease die before turning three years of age due to the complications that arise from this condition. Objective: Review the clinical symptomatology of this disease and the neurocognitive alterations that occurred in 145 cases of patients with HSAN IV reported in the scientific literature between 2000 and 2017. Findings: The review allowed to identify the most frequent clinical symptoms in patients with HSAN IV: fever, anhidrosis, osteomyelitis, fractures, arthropathies and avascular necrosis. Conclusions: There is a scientific ignorance of the impact of HSAN IV on the behavior and superior functions in patients affected by this disease. © 2020, Universidad del Norte. All rights reserved.spa
dc.format.extent18 páginas
dc.format.mimetypeapplication/pdfspa
dc.language.isospaspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceRevista Salud Uninortespa
dc.titleClinical manifestations of congenital insensitivity to pain with anhidrosisspa
dc.title.alternativeManifestaciones clínicas de la insensibilidad congénita al dolor con anhidrosisspa
dcterms.bibliographicCitationDyck, P.J., Mellinger, J.F., Reagan, T.J., Horowitz, S.J., Mcdonald, J.W., Litchy, W.J., Daube, J.R., (...), Lambert, E.H. Not 'indifference to pain' but varieties of hereditary sensory and autonomic neuropathy (1983) Brain, 106 (2), pp. 373-390. Cited 154 times. doi: 10.1093/brain/106.2.373spa
dcterms.bibliographicCitationLePlat, M. Dictionnaire de Médecine en 30 volumes 1846. Cited 2 times. Parisspa
dcterms.bibliographicCitationDearborn, F. (2005) Enfermedades de la piel incluyendo los exhantemas India: B. Jain Publishersspa
dcterms.bibliographicCitationLa vanguardia. Un enigma fisiologico “El Acerico humano, p. 6.spa
dcterms.bibliographicCitationIndo, Y. Congenital Insensitivity to Pain with Anhidrosis (2014) GeneReviews. Cited 41 times. Disponible de http://www.ncbi.nlm.nih.gov/books/NBK1769/spa
dcterms.bibliographicCitationLee, S.-T., Lee, J., Lee, M., Kim, J.-W., Ki, C.-S. Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis (2009) Muscle and Nerve, 40 (5), pp. 855-859. Cited 23 times. http://www3.interscience.wiley.com/cgi-bin/fulltext/122515463/PDFSTART doi: 10.1002/mus.21340spa
dcterms.bibliographicCitationKucukdurmaz, F., Imren, Y., Uruc, V., Sen, C. Dcongenital insensitivity to pain with anhidrosis (CIPA) manifested with chronic osteomyelitis; a case report (Open Access) (2015) Journal of Clinical and Analytical Medicine, 6 (2), pp. 230-232. Cited 5 times. http://www.jcam.com.tr/files/KATD-912.pdf doi: 10.4328/JCAM.912spa
dcterms.bibliographicCitationOrlandi, M. Hiperhidrosis: una patología con solución (2003) Folia Dermatol Perú, 14 (3), pp. 35-38. Cited 2 times.spa
dcterms.bibliographicCitationPinacho-Velázquez, J.L. Heat stroke in the children (2014) Revista Mexicana de Pediatria, 81 (3), pp. 115-119. Cited 2 times. http://www.medigraphic.com/pdfs/pediat/sp-2014/sp143h.pdfspa
dcterms.bibliographicCitationDearborn, Frederick (2005) Enfermedades de la piel, incluyendo los exhantemas India: B. Jain Publishersspa
dcterms.bibliographicCitationDaneshjou, K., Jafarieh, H., Raaeskarami, S.-R. Congenital insensitivity to pain and anhydrosis (CIPA) syndrome; A report of 4 cases (2012) Iranian Journal of Pediatrics, 22 (3), pp. 412-416. Cited 23 times. http://ijp.tums.ac.ir/index.php/ijp/article/view/1464/pdfspa
dcterms.bibliographicCitationKarimi, M., Fallah, R. A case report of congenital insensitivity to pain and anhidrosis (CIPA) (2012) Iranian Journal of Child Neurology, 6 (3), pp. 45-48. Cited 5 times.spa
dcterms.bibliographicCitationMakonahalli, R., Seneviratne, J., Seneviratne, U. Acute small fiber neuropathy following mycoplasma infection: A rare variant of guillain-barré syndrome (2014) Journal of Clinical Neuromuscular Disease, 15 (4), pp. 147-151. Cited 9 times. http://journals.lww.com/jcnmd doi: 10.1097/CND.0000000000000031spa
dcterms.bibliographicCitationCallea, M., Yavuz, I., Clarich, G., Cammarata-Scalisi, F. Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia (2015) Archivos Argentinos de Pediatria, 113 (6), pp. e341-e344. Cited 4 times. http://www.scielo.org.ar/pdf/aap/v113n6/v113n6a27.pdf doi: 10.5546/aap.2015.e341spa
dcterms.bibliographicCitationCarrillo, M, Aguilar, P, Rico, G., Arenas, R. Displasia ectodérmica anhidrótica: informe de 3 casos suges-tivos de herencia ligada al cromosoma x (2014) Dermotología CMQ, 12 (3), pp. 175-178.spa
dcterms.bibliographicCitationMarín Botero, M.L., Espinal Botero, G., Arroyo Fuentes, T.M., Posso Zapata, M.V., David Pérez, M., Castañeda Peláez, D.A., Sierra Pérez, J.I. Hypohydrotic ectodermal dysplasia: Report of cases (2013) Avances en Odontoestomatologia, 29 (1), pp. 11-23. Cited 2 times. http://scielo.isciii.es/pdf/odonto/v29n1/original1.pdf doi: 10.4321/S0213-12852013000100002spa
dcterms.bibliographicCitationXavier, M.H.S.B., Porto, F.H.D.G., Pereira, G.B., Quevedo, L.P., De Freitas, P.M., Do Nascimento, O.J.M., De Freitas, M.R.G. Anhidrosis as the first sign of Ross syndrome (Open Access) (2009) Arquivos de Neuro-Psiquiatria, 67 (2 B), pp. 505-506. Cited 5 times. http://www.scielo.br/pdf/anp/v67n2b/v67n2ba25.pdf doi: 10.1590/S0004-282X2009000300025spa
dcterms.bibliographicCitationWolff, K, Goldsmith, L, Katz, S, Gilchrest, B, Paller, A, Leffell, D. (2009) Dermatología en medicina general, 2. (7a ed., España: Panamericanaspa
dcterms.bibliographicCitationRotthier, A., Baets, J., Vriendt, E.D., Jacobs, A., Auer-Grumbach, M., Lévy, N., Bonello-Palot, N., (...), Timmerman, V. Genes for hereditary sensory and autonomic neuropathies: A genotype-phenotype correlation (2009) Brain, 132 (10), pp. 2699-2711. Cited 133 times. http://brain.oxfordjournals.org/ doi: 10.1093/brain/awp198spa
dcterms.bibliographicCitationTüysüz, B., Bayrakli, F., Diluna, M.L., Bilguvar, K., Bayri, Y., Yalcinkaya, C., Bursali, A., (...), Gunel, M. Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: Demonstration of a founder mutation in the Turkish population (2008) Neurogenetics, 9 (2), pp. 119-125. Cited 17 times. doi: 10.1007/s10048-008-0121-9spa
dcterms.bibliographicCitationKilic, S.S., Ozturk, R., Sarisozen, B., Rotthier, A., Baets, J., Timmerman, V. Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis (Open Access) (2009) Neurogenetics, 10 (2), pp. 161-165. Cited 19 times. doi: 10.1007/s10048-008-0165-xspa
dcterms.bibliographicCitationAzadvari, M., Emami Razavi, S.Z., Kazemi, S. Hereditary sensory and autonomic neuropathy type IV in 9 year old boy: A case report (2016) Iranian Journal of Child Neurology, 10 (2), pp. 83-85. Cited 4 times. http://journals.sbmu.ac.ir/index.php/ijcn/article/download/9798/8828spa
dcterms.bibliographicCitationMachtei, A., Levy, J., Friger, M., Bodner, L. Osteomyelitis of the mandible in a group of 33 pediatric patients with congenital insensitivity to pain with anhidrosis (2011) International Journal of Pediatric Otorhinolaryngology, 75 (4), pp. 523-526. Cited 19 times. doi: 10.1016/j.ijporl.2011.01.011spa
dcterms.bibliographicCitationOfluoğlu, D, Altın, N, Yaman, E, Tuna, E, Aytepe, Z, Tanyeri, H. Oral manifestations and prosthetic rehabilitation In hereditary sensory and autonomic neuropathy (hsan) type iv: a case report (2016) J Istanbul Univ Fac Dent, 50 (2), pp. 49-53. Cited 4 times. dx.doi.orgspa
dcterms.bibliographicCitationLevy Erez, D., Levy, J., Friger, M., Aharoni-Mayer, Y., Cohen-Iluz, M., Goldstein, E. Assessment of cognitive and adaptive behaviour among individuals with congenital insensitivity to pain and anhidrosis (Open Access) (2010) Developmental Medicine and Child Neurology, 52 (6), pp. 559-562. Cited 26 times. doi: 10.1111/j.1469-8749.2009.03567.xspa
dcterms.bibliographicCitationNorcliffe-Kaufmann, L., Katz, S.D., Axelrod, F., Kaufmann, H. Norepinephrine deficiency with normal blood pressure control in congenital insensitivity to pain with anhidrosis (2015) Annals of Neurology, 77 (5), pp. 743-752. Cited 20 times. http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8249 doi: 10.1002/ana.24377spa
dcterms.bibliographicCitationBeigelman, A., Levy, J., Hadad, N., Pinsk, V., Haim, A., Fruchtman, Y., Levy, R. Abnormal neutrophil chemotactic activity in children with congenital insensitivity to pain with anhidrosis (CIPA): The role of nerve growth factor (2009) Clinical Immunology, 130 (3), pp. 365-372. Cited 31 times. doi: 10.1016/j.clim.2008.09.005spa
dcterms.bibliographicCitationIftikhar, S., Javed, M.A. Seeing is not always believing: Congenital insensitivity to pain with anhidrosis mimicking leprosy (2013) Mayo Clinic Proceedings, 88 (12), pp. e153-e154. Cited 3 times. http://www.journals.elsevier.com/mayo-clinic-proceedings doi: 10.1016/j.mayocp.2013.02.018spa
dcterms.bibliographicCitationManor, E., Joshua, B.Z., Levy, J., Brennan, P.A., Bodner, L. Pathological fracture of the mandible in a paediatric patient with congenital insensitivity to pain with anhidrosis (CIPA) (2013) Journal of Cranio-Maxillofacial Surgery, 41 (2), pp. e39-e41. Cited 6 times. doi: 10.1016/j.jcms.2012.07.008spa
dcterms.bibliographicCitationBakri, F, Wahbeh, A, Abu Seina, A, Al Khader, A, Obeidat, F, Alawwa, I, Masri, A. Congenital insensitivity to pain and anhydrosis due to a rare mutation and that is complicated by inflammatory bowel disease and amyloidosis: a case report (2016) Clinical case reports, 4 (10), pp. 997-1000. Cited 4 times.spa
dcterms.bibliographicCitationSayyahfar, S., Chavoshzadeh, Z., Khaledi, M., Madadi, F., Yeganeh, M.H., Sawamura, D., Nakano, H., (...), Rezaei, N. Congenital insensitivity to pain with anhidrosis presenting with palmoplantar keratoderma (2013) Pediatric Dermatology, 30 (6), pp. 754-756. Cited 10 times. doi: 10.1111/j.1525-1470.2012.01833.xspa
dcterms.bibliographicCitationSaleh-Gohari, N., Mohammadi-Anaie, M. Congenital insensitivity to pain with anhidrosis in an Iranian Patient (2013) Basic and Clinical Neuroscience, 4 (1), pp. 88-90. Cited 3 times. http://bcn.tums.ac.ir/browse.php?a_id=314&slc_lang=en&sid=1&ftxt=1spa
dcterms.bibliographicCitationGupta, B. Congenital insensitivity of pain with anhidrosis (2003) Indian Journal of Pediatrics, 70 (1), pp. 109-111. Cited 10 times. http://www.springerlink.com/content/0019-5456 doi: 10.1007/BF02722757spa
dcterms.bibliographicCitationAltassan, R., Saud, H.A., Masoodi, T.A., Dosssari, H.A., Khalifa, O., Al-Zaidan, H., Sakati, N., (...), Wakil, S.M. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype (2017) American Journal of Medical Genetics, Part A, 173 (4), pp. 1009-1016. Cited 17 times. http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4833 doi: 10.1002/ajmg.a.38120spa
dcterms.bibliographicCitationAshwin, D.P., Chandan, G.D., Jasleen, H.K., Rajkumar, G.C., Rudresh, K.B., Prashanth, R. Hereditary sensory and autosomal peripheral neuropathy-type IV: case series and review of literature (2015) Oral and Maxillofacial Surgery, 19 (2), pp. 117-123. Cited 11 times. www.springer.com/medicine/surgery/journal/10006 doi: 10.1007/s10006-015-0486-5spa
dcterms.bibliographicCitationYang, L., Ji, S.F., Yue, R.J., Cheng, J.L., Niu, J.J. Old fractures in two patients with congenital insensitivity to pain with anhidrosis: Radiological findings (2013) Clinical Imaging, 37 (4), pp. 788-790. Cited 3 times. doi: 10.1016/j.clinimag.2013.01.016spa
dcterms.bibliographicCitationAmano, S., Fukuoka, S., Usui, T., Honda, N., Ideta, R., Ochiai, M., Yamagami, S., (...), Awaya, Y. Ocular manifestations of congenital insensitivity to pain with anhidrosis (2006) American Journal of Ophthalmology, 141 (3), pp. 472-477. Cited 22 times. doi: 10.1016/j.ajo.2005.10.016spa
dcterms.bibliographicCitationDias, E., Charki, S. Congenital insensitivity to pain with anhidrosis (2012) Journal of Pediatric Neurosciences, 7 (2), pp. 156-157. Cited 2 times. doi: 10.4103/1817-1745.102593spa
dcterms.bibliographicCitationPrashanth, G.P., Kamate, M. A case of hereditary sensory autonomic neuropathy type IV (2012) Annals of Indian Academy of Neurology, 15 (2), pp. 134-136. Cited 5 times. doi: 10.4103/0972-2327.94999spa
dcterms.bibliographicCitationSinha, R., John, B., Raju, U., Singh, D., Sodhi, K. A rare case of congenital insensitivity to pain and anhidrosis with seizure disorder (2011) Journal of Pediatric Neurology, 9 (2), pp. 247-249. https://www.thieme-connect.com/products/ejournals/journal/10.1055/s-00029030 doi: 10.3233/JPN-2011-0470spa
dcterms.bibliographicCitationTanaka, T., Satoh, T., Tanaka, A., Yokozeki, H. Congenital insensitivity to pain with anhidrosis: A case with preserved itch sensation to histamine and partial pain sensation (2012) British Journal of Dermatology, 166 (4), pp. 888-891. Cited 15 times. doi: 10.1111/j.1365-2133.2011.10706.xspa
dcterms.bibliographicCitationWang, Q.-L., Guo, S., Duan, G., Ying, Y., Huang, P., Liu, J.Y., Zhang, X. Phenotypes and Genotypes in Five Children with Congenital Insensitivity to Pain with Anhidrosis (Open Access) (2016) Pediatric Neurology, 61, pp. 63-69. Cited 17 times. www.elsevier.com/locate/pedneu doi: 10.1016/j.pediatrneurol.2016.04.006spa
dcterms.bibliographicCitationShin, J.Y., Kim, S.-W., Roh, S.-G., Lee, N.-H., Yang, K.-M. Congenital insensitivity to pain and anhidrosis (2016) Archives of Plastic Surgery, 43 (1), pp. 95-97. Cited 4 times. http://www.e-aps.org/Synapse/Data/PDFData/2023APS/aps-43-95.pdf doi: 10.5999/aps.2016.43.1.95spa
dcterms.bibliographicCitationVan Den Bosch, G.E., Baartmans, M.G.A., Vos, P., Dokter, J., White, T., Tibboel, D. Pain insensitivity syndrome misinterpreted as inflicted burns (Open Access) (2014) Pediatrics, 133 (5), pp. e1381-e1387. Cited 25 times. http://pediatrics.aappublications.org/content/133/5/e1381.full.pdf+html doi: 10.1542/peds.2013-2015spa
dcterms.bibliographicCitationKurth, I., Baumgartner, M., Schabhüttl, M., Tomni, C., Windhager, R., Strom, T.M., Wieland, T., (...), Auer-Grumbach, M. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy (2016) American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 171 (6), pp. 875-878. Cited 8 times. http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-485X doi: 10.1002/ajmg.b.32458spa
dcterms.bibliographicCitationBachiocco, V., Rosalba, B., Cristina, M.M., Gabriele, B. Sensory phenotype assessment in a young girl affected by congenital insensitivity to pain (CIPA) (2007) Paediatric Anaesthesia, 17 (11), pp. 1105-1110. Cited 5 times. http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1460-9592 doi: 10.1111/j.1460-9592.2007.02338.xspa
dcterms.bibliographicCitationNolano, M., Crisci, C., Santoro, L., Barbieri, F., Casale, R., Kennedy, W.R., Wendelschafer-Crabb, G., (...), Caruso, G. Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis (2000) Clinical Neurophysiology, 111 (9), pp. 1596-1601. Cited 110 times. doi: 10.1016/S1388-2457(00)00351-5spa
dcterms.bibliographicCitationRaspall-Chaure, M., Del Toro-Riera, M., Gratacós, M., Cuenca-León, E., Ferrer, I., Indo, Y., Roig-Quilis, M., (...), Macaya-Ruiz, A. Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome (2005) Revista de Neurologia, 41 (4), pp. 218-222. Cited 8 times. http://www.neurologia.com/pdf/Web/4104/t040218.pdf doi: 10.33588/rn.4104.2005011spa
dcterms.bibliographicCitationCampos, A, Martínez, J, De la Riva, V. Insensibilidad congénita al dolor con anhidrosis asociado a osteo-mielitis mandibular (2012) Revista Mexicana de Cirugia bucal y Maxilofacial, 8 (1), pp. 18-22. Cited 2 times.spa
dcterms.bibliographicCitationAlbuja Echeverría, B.O., Alvear Lozano, M.B., Ordóñez Paredes, C.P. Congenital insensitivity to pain with anhidrosis. Clinical diagnosis, evolution and complications. Case report (2014) Archivos Argentinos de Pediatria, 112 (5), pp. e200-e205. Cited 4 times. http://www.scielo.org.ar/pdf/aap/v112n5/v112n5a14.pdf doi: 10.5546/aap.2014.e200spa
dcterms.bibliographicCitationSchalka, M.M.S., Corrêa, M.S.N.P., Ciamponi, A.L. Congenital insensitivity-to-pain with anhidrosis (CIPA): A case report with 4-year follow-up (2006) Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, 101 (6), pp. 769-773. Cited 23 times. doi: 10.1016/j.tripleo.2005.07.030spa
dcterms.bibliographicCitationSathiaseelan, S., Rayar, U. The mystery of the broken bones (2003) CMAJ. Canadian Medical Association Journal, 169 (11), pp. 1189-1190. Cited 5 times. http://www.cmaj.ca/spa
dcterms.bibliographicCitationAcosta-G, A, Bogantes-L, S. Neuropatía autonómica sensorial hereditaria (2014) Caso Clínico. Acta méd costa-rric, 56 (2), pp. 81-84.spa
dcterms.bibliographicCitationMcKelvey, L., Shorten, G.D., O'Keeffe, G.W. Nerve growth factor-mediated regulation of pain signalling and proposed new intervention strategies in clinical pain management (Open Access) (2013) Journal of Neurochemistry, 124 (3), pp. 276-289. Cited 116 times. doi: 10.1111/jnc.12093spa
dcterms.bibliographicCitationMurphy, S.M., Laurá, M., Reilly, M.M. DNA testing in hereditary neuropathies (2013) Handbook of Clinical Neurology, 115, pp. 213-232. Cited 9 times. http://www.sciencedirect.com/science/journal/00729752 doi: 10.1016/B978-0-444-52902-2.00012-6spa
dcterms.bibliographicCitationPierotti, M.A., Greco, A. Oncogenic rearrangements of the NTRK1/NGF receptor (Open Access) (2006) Cancer Letters, 232 (1), pp. 90-98. Cited 75 times. doi: 10.1016/j.canlet.2005.07.043spa
dcterms.bibliographicCitationHaga, N., Kubota, M., Miwa, Z. Epidemiology of hereditary sensory and autonomic neuropathy type IV and V in Japan (2013) American Journal of Medical Genetics, Part A, 161 (4), pp. 871-874. Cited 22 times. doi: 10.1002/ajmg.a.35803spa
dcterms.bibliographicCitationRosemberg, S., Nagahashi Marie, S.K., Kliemann, S. Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV) (Open Access) (1994) Pediatric Neurology, 11 (1), pp. 50-56. Cited 168 times. doi: 10.1016/0887-8994(94)90091-4spa
dcterms.bibliographicCitationToscano, E., Simonati, A., Indo, Y., Andria, G. No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V (Open Access) (2002) Annals of Neurology, 52 (2), pp. 224-227. Cited 23 times. doi: 10.1002/ana.10245spa
dcterms.bibliographicCitationDanziger, N., Prkachin, K.M., Willer, J.-C. Is pain the price of empathy? The perception of others' pain in patients with congenital insensitivity to pain (Open Access) (2006) Brain, 129 (9), pp. 2494-2507. Cited 123 times. http://brain.oxfordjournals.org/ doi: 10.1093/brain/awl155spa
dcterms.bibliographicCitationSantoya-Montes, YE, Zequeira, R, Gutiérrez-Ruiz, K. Funcionamiento Cognitivo Global y Conducta Adaptativa en dos Niñas con Neuropatía Sensitiva Autonómica Hereditaria Tipo IV (2018) Rev. Chil. Neurop-sicol, 13 (2), pp. 46-51. Cited 2 times. 61spa
dcterms.bibliographicCitationSantoya-Montes, YE, Gutiérrez-Ruiz, K, Puentes-Rozo, P, Rojas-Martinez, J. Executive functioning in two patients with Hereditary Sensory Autonomic Neuropathy: Single case study (2018) Journal of the International Neuropsychological Society, 24 (s2), p. 178. doi.orgspa
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dc.identifier.doihttp://dx.doi.org/10.14482/sun.36.1.616.56
dc.subject.keywordsHereditary Sensory and Autonomic Neuropathies;spa
dc.subject.keywordsCongenital Analgesia;spa
dc.subject.keywords1-Deoxysphingolipidspa
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dc.identifier.instnameUniversidad Tecnológica de Bolívarspa
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