- Hereditary Sensory Neuropathy Type 2 (Congenital sensory neuropathy): A case report
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Lee HK, Limb WS, Ahn BW
- KMID: 2461800
- J Korean Orthop Assoc.
- 1977 Sep;12(3):499-505.
- doi: 10.4055/jkoa.1977.12.3.499
Hereditary sensory neuropathy is a unusual disease which is charcterized by mutilating acropathy with cutaneous sensory loss and complete absence of sensory apparatus. We experienced a case of bereditary sensory... -
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- Genetics of Hereditary Peripheral Neuropathies
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Cho SY, Choi BO
- KMID: 2244889
- J Genet Med.
- 2009 Jun;6(1):25-37.
Hereditary peripheral neuropathies can be categorized as hereditary motor and sensory neuropathies (HMSN), hereditary motor neuropathies (HMN), and hereditary sensory neuropathies (HSN). HMSN, HMN, and HSN are further subdivided into... -
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- Ultrastructural Findings of Hereditary Sensory and Autonomic Neuropathies, Type IV and II
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Go JH, Suh YL
- KMID: 2275734
- Korean J Pathol.
- 1998 Jul;32(7):535-539.
Hereditary sensory and autonomic neuropathies (HSAN) are disorders of hereditary neuropathy mainly affecting sensation and also accompanying autonomic nervous system dysfunction. They are divided into five subtypes based on inheritance... -
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- A Case of Hereditary Sensory Neuropathy Type II with Acroosteolysis
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Seo JH, Song CH, Park CS, Lee CH, Lee JS, Kim TS, Lee SK
- KMID: 1542342
- J Korean Rheum Assoc.
- 1997 Jan;4(1):105-110.
The hereditary sensory neuropathy is a very rare disease characterized by prominent sensory loss without corresponding motor involvement, but may be associated with autonomic features. Currently, the disease is divided... -
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- Two Novel Mutations in the HSN2 Gene Identified in a Korean Patients with Hereditary Sensory Autonomic Neuropathy Type II
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Bae JS, Cho HJ, An JY, Kim BJ, Ki CS
- KMID: 1527879
- J Korean Neurol Assoc.
- 2007 May;25(2):251-254.
A 38-year-old Korean man was diagnosed with hereditary sensory and autonomic neuropathy (HSAN) type 2 because of his chronic sensory neuropathy and progressive acro-mutilation. Genetic analysis revealed that he was... -
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- A Case of Congenital Insensitivity to Pain with Anhidrosis
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Lee M, Beck NS, Jin D, Suh YL
- KMID: 2208075
- J Korean Pediatr Soc.
- 1997 Nov;40(11):1621-1621.
Congenital insensitivity to pain with anhidrosies (CIPA) is one of the exceedingly rare hereditary sensory autonomic neuropathies (HSAN). There are five types of HSAN according to hereditary transmission, natural history,... -
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- Total Intravenous Anesthetic Management of a Child with Congenital Insensitivity to Pain with Anhidrosis : A case report
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Lee SJ, Kim YK, Seong KW, Kim SW
- KMID: 1937607
- Korean J Anesthesiol.
- 2007 Mar;52(3):367-370.
- doi: 10.4097/kjae.2007.52.3.367
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare hereditary sensory and autonomic neuropathy. CIPA is characterized by inability to sweat, insensitivity to pain, self-mutilation, recurrent episodes of hyperpyrexia,... -
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- Congenital Insensitivity to Pain and Anhidrosis Masquerading as a Chronic Osteomyelitis of the Talus: A Case Report
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Shin YW, Chung HJ, Oh JS
- KMID: 1469368
- J Korean Foot Ankle Soc.
- 2009 Dec;13(2):203-206.
We experienced a case of congenital insensitivity to pain with anhidrosis mimicking a chronic osteomyelitis of the talus, with recurrent ankle swelling and intermittent fever. He was misdiagnosed as low... -
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- Seropositive rheumatoid arthritis in a female patient with sensory neuropathy
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Kim KJ
- KMID: 1794637
- Korean J Intern Med.
- 2014 Sep;29(5):683-684.
- doi: 10.3904/kjim.2014.29.5.683
No abstract available. -
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- Complication of Lateral Condyle Fracture of Humerus in a Patient with Hereditary Sensory Autonomic Neuropathy Type IV: A Case Report
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Kang HJ, Sung SY, Shin SJ, Park HW
- KMID: 2042256
- J Korean Orthop Assoc.
- 1999 Dec;34(6):1175-1178.
Hereditory Sensory Automnomic Neuropathy (HSAN) is a rare disorder. Five types of HSAN have been described by Dyck et al. Congenital insensitivity to pain with anhidrosis is classified HSAN Type... -
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- Congenital Insensitivity to Pain with Anhidrosis: Five-Year-Old Girl with a Neglected Distal Femur Fracture
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Woo SH, Kim TW, Bae JY, Kwak SH
- KMID: 2461238
- J Korean Orthop Assoc.
- 2019 Oct;54(5):463-468.
- doi: 10.4055/jkoa.2019.54.5.463
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare disease that affects the sensory and autonomic nervous system. The patients do not have the ability to sense different sensations,... -
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- A case report of congenital sensory neuropathy with anhidrosis
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Lee WH, Lee SH, Ha SW, Chang HS, Lee DY, Han MC
- KMID: 2345964
- J Korean Radiol Soc.
- 1974 Dec;10(2):238-241.
- doi: 10.3348/jkrs.1974.10.2.238
Congenital sensory neuropathy with anhidrosis is rare disease and may be confused with other cause of paininsensitivity or difference. Other causes of pain insensitivity include congenital indifference to pain,congenital sensory... -
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- Anesthetic management of patient with congenital insensitivity to pain with anhidrosis (CIPA) by using BIS monitor: A case report
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Jo JK, Lim YH, Kim HJ, Yon JH, Woo SH, Kim KM
- KMID: 2116982
- Anesth Pain Med.
- 2011 Apr;6(2):186-190.
Congenital insensitivity to pain with anhidrosis (CIPA, or hereditary sensory and autonomic neuropathy type IV) is a rare, autosomal recessive disease, is characterized by inability to sweat, insensitivity to pain,... -
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- Congenital insensitivity to pain and anhidrosis with selective loss of unmyelinated fiber (Hereditory sensory autonomic neuropathy IV)
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Son IH, Cho SJ, Moon JS, Park YK, Lee SS, Kim SM, Sunwoo IN
- KMID: 2342603
- J Korean Neurol Assoc.
- 1997 Feb;15(1):211-215.
Hereditory Sensory Autonomic Neuropathy(HSAN) is variable rare disorder. So the classification of HSAN could be somewhat unsettled. There are intermingled overlap variants of HSAN in view of clinical manifestations and... -
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- Congenital Insensitivity to Pain with Anhidrosis: Follow-up of 1 case
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Choi ES, Lee YS, Yang SH, Shin JN, Kim YS, Jung KH
- KMID: 2323156
- J Korean Acad Rehabil Med.
- 1998 Oct;22(5):1151-1155.
Congenital insensitivity to pain with anhidrosis (CIPA: a hereditary sensory and autonomic neuropathy, HSAN IV) is a rare disease characterized by the self-mutilation, bone fracture, multiple scars, osteomyelitis, joint deformities... -
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- A novel mutation in the DNMT1 gene in a patient presenting with pure cerebellar ataxia
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Algahtani , Shirah B
- KMID: 2401809
- J Genet Med.
- 2017 Dec;14(2):71-74.
- doi: 10.5734/JGM.2017.14.2.71
Mutations in the DNA methyltransferase 1 gene (DNMT1) were reported to cause two phenotypes: OMIM 604121 and OMIM 614116. The first phenotype includes autosomal dominant cerebellar ataxia, deafness, and narcolepsy,... -
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- Anesthetic Management in a Patient with Congenital Insensitivity to Pain with Anhidrosis: A case report
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Jang YH, Park JH, Song KS
- KMID: 2237544
- Korean J Anesthesiol.
- 2004 Aug;47(2):281-283.
- doi: 10.4097/kjae.2004.47.2.281
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare inherited disease, which affects a patient's pain sensation and thermoregulation. There are several anesthetic considerations for those with this disorder.... -
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- Anesthetic Management for a Patient with Congenital Insensitivity to Pain with Anhidrosis (CIPA): A case report
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Kim SJ, Yoo KY, Kang MW, Hong JW, Lee HG, Shin DJ, Kim WM
- KMID: 2239839
- Korean J Anesthesiol.
- 2008 Mar;54(3):S47-S50.
- doi: 10.4097/kjae.2008.54.3.S47
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare, autosomal-recessive disorder characterized by the clinical triad of indifference of pain, anhidrosis and heat intolerance.Because of their lack of autonomic... -
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- Dental Management in a Patient with Congenital Insensitivity to Pain with Anhidrosis : A Case Report
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Bae C, Lee D, Kim J, Yang Y
- KMID: 2467078
- J Korean Acad Pediatr Dent.
- 2019 Nov;46(4):416-421.
- doi: 10.5933/JKAPD.2019.46.4.416
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare, autosomal recessive disorder; affected patients are characterized by inability to feel pain and to sweat over the entire body, as... -
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- A Case of Pressure Sore in Congenital Insensitivity to Pain with Anhidrosis
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Hwang JH, Park SH, Yoo SI, Noh BK, Kim ES, Kim KS, Lee SY
- KMID: 2120148
- J Korean Soc Plast Reconstr Surg.
- 2006 Sep;33(5):669-671.
PURPOSE: Congenital insensitivity to pain with anhidrosis(CIPA) is a rare form of autosomal recessive peripheral sensory neuropathy. Patients with CIPA show loss of pain sensation, which leads to corneal ulcers... -
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