Congenital insensitivity to pain: Case report of a rare entity
Hereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by insensitivity to noxious stimuli and autonomic dysfunction, associated with pathological abnormalities of the peripheral nerves. Five types of HSAN have been reported in literature, out of which Type V kn...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2018-01-01
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| Series: | Indian Journal of Paediatric Dermatology |
| Subjects: | |
| Online Access: | http://www.ijpd.in/article.asp?issn=2319-7250;year=2018;volume=19;issue=1;spage=48;epage=50;aulast=Dahiya |
| _version_ | 1818541215198478336 |
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| author | Swati Dahiya Kondajji Ramchandra Vijayalakshmi Mubeen Khan |
| author_facet | Swati Dahiya Kondajji Ramchandra Vijayalakshmi Mubeen Khan |
| author_sort | Swati Dahiya |
| collection | DOAJ |
| description | Hereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by insensitivity to noxious stimuli and autonomic dysfunction, associated with pathological abnormalities of the peripheral nerves. Five types of HSAN have been reported in literature, out of which Type V known as congenital insensitivity to pain (CIP) is a rare autosomal recessive condition. Self-mutilation is an invariable feature of this disorder, involving the teeth and orofacial structures. This case report describes a case of a 6-year-old girl with CIP brought by her parents for prostheses to replace her self-extracted primary teeth. |
| first_indexed | 2024-12-11T22:05:41Z |
| format | Article |
| id | doaj.art-01b6a472b98848ebaf7a1dbda547679f |
| institution | Directory Open Access Journal |
| issn | 2319-7250 |
| language | English |
| last_indexed | 2024-12-11T22:05:41Z |
| publishDate | 2018-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Indian Journal of Paediatric Dermatology |
| spelling | doaj.art-01b6a472b98848ebaf7a1dbda547679f2022-12-22T00:48:58ZengWolters Kluwer Medknow PublicationsIndian Journal of Paediatric Dermatology2319-72502018-01-01191485010.4103/ijpd.IJPD_142_16Congenital insensitivity to pain: Case report of a rare entitySwati DahiyaKondajji Ramchandra VijayalakshmiMubeen KhanHereditary sensory and autonomic neuropathies (HSANs) are a group of disorders characterized by insensitivity to noxious stimuli and autonomic dysfunction, associated with pathological abnormalities of the peripheral nerves. Five types of HSAN have been reported in literature, out of which Type V known as congenital insensitivity to pain (CIP) is a rare autosomal recessive condition. Self-mutilation is an invariable feature of this disorder, involving the teeth and orofacial structures. This case report describes a case of a 6-year-old girl with CIP brought by her parents for prostheses to replace her self-extracted primary teeth.http://www.ijpd.in/article.asp?issn=2319-7250;year=2018;volume=19;issue=1;spage=48;epage=50;aulast=DahiyaCongenitaloral manifestationspain |
| spellingShingle | Swati Dahiya Kondajji Ramchandra Vijayalakshmi Mubeen Khan Congenital insensitivity to pain: Case report of a rare entity Indian Journal of Paediatric Dermatology Congenital oral manifestations pain |
| title | Congenital insensitivity to pain: Case report of a rare entity |
| title_full | Congenital insensitivity to pain: Case report of a rare entity |
| title_fullStr | Congenital insensitivity to pain: Case report of a rare entity |
| title_full_unstemmed | Congenital insensitivity to pain: Case report of a rare entity |
| title_short | Congenital insensitivity to pain: Case report of a rare entity |
| title_sort | congenital insensitivity to pain case report of a rare entity |
| topic | Congenital oral manifestations pain |
| url | http://www.ijpd.in/article.asp?issn=2319-7250;year=2018;volume=19;issue=1;spage=48;epage=50;aulast=Dahiya |
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