- Efficacy of Stellate Ganglion Block in Cholinergic Urticaria with Acquired Generalized Hypohidrosis
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Shin JH, Kim DW, Yang JY, Lee WI
- KMID: 2278172
- Korean J Pain.
- 2012 Oct;25(4):278-280.
- doi: 10.3344/kjp.2012.25.4.278
Cholinergic urticaria with acquired generalized hypohidrosis, and its pathophysiology is not well known. Autoimmunity to sweat glands or to acetylcholine receptors on sweat glands has been mentioned as one of... -
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- Predictive value of cobalt chloride solution for hypohidrosis with topiramate
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Lee H, Lee SH, Kim SJ
- KMID: 2280065
- Korean J Pediatr.
- 2006 Nov;49(11):1180-1185.
- doi: 10.3345/kjp.2006.49.11.1180
PURPOSE: The aims of this study were to verify the incidence of hypohidrosis and to determine the predictive value of noninvasive indicator test (Neurocheck(TM)) for sweating after administration of topiramate... -
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- Idiopathic Segmental Anhidrosis with Hyporeflexia: Incomplete Ross Syndrome
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Kang MS, Jung HR, Lee H, Kim HA
- KMID: 2129329
- J Korean Neurol Assoc.
- 2015 Nov;33(4):343-345.
- doi: 10.17340/jkna.2015.4.20
No abstract available. -
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- Neurological Disorders Associated with Sweating
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Park KJ
- KMID: 2203108
- J Korean Soc Clin Neurophysiol.
- 2012 Jun;14(1):12-19.
Thermoregulatory sweat is principal mean for homeostasis of temperature. Sweat glands have eccrine gland, apocrine gland, and apoeccrine glands. Disorders of sweating are manifested by excess (hyperhidrosis) or deficit (hypohidrosis,... -
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- Hypohidrotic Ectodermal Dysplasia with Congenital Cataract and Corneal Opacity: Report of a Case
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Cho OJ, Lee SW
- KMID: 1678307
- Korean J Dermatol.
- 1981 Aug;19(4):583-588.
Hereditary hypohidrotic ectodermal dysplasia is a genodermatosis that demonstrates in its typical form a triad of hypohidrosis, hypotrichosis, and hypodontia Despite marked abnormalities of ectodermal structures, reports of cataract and... -
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- Two Cases with Bilateral Adie's Pupils
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Kim BJ, Lee SK, Lee WY, Roh JK, Lee SB, Myung H, Han SH
- KMID: 2016056
- J Korean Neurol Assoc.
- 1990 Jun;8(1):92-97.
Adie's tonic pupil usually consists of mydriasis, defect in accommodation. Poor or absent light reflex, and tonic near reflex, It is usually unilateral, but rarelY observed bilaterally. The pupillary abnormalities... -
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- Hypohidrotic Ectodermal Dysplasia
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Shin SW, Cha SH, Oh YK, Park SD
- KMID: 2086205
- Korean J Dermatol.
- 1999 Feb;37(2):267-272.
Congenital hypohidrotic ectodermal dysplasia is a rare genodermatosis. It is characterized by hypohidrosis hypotrichosis, dental hypoplasia and characterstic facial features, which reflect a wide constellation of developmental defec of tissue... -
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- Congenital insensitivity to pain with anhidrosis: a case report
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Kim JS, Woo YJ, Kim GM, Kim CJ, Ma JS, Hwang TJ, Lee MC
- KMID: 1731324
- J Korean Med Sci.
- 1999 Aug;14(4):460-464.
- doi: 10.3346/jkms.1999.14.4.460
Congenital insensitivity to pain with anhidrosis (CIPA) is a very rare genetic disorder of the peripheral nervous system characterized by recurrent episodes of unexplained fever, generalized anhidrosis, insensitivity to pain... -
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- A Case of Familial Basaloid Follicular Hamartoma Syndrome
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Lee HJ, Lee WJ, Chang SE, Lee MW, Moon KC, Choi JH, Koh JK
- KMID: 2302143
- Korean J Dermatol.
- 2007 Oct;45(10):1070-1073.
Basaloid follicular hamartoma is a benign adnexal tumor consisting of basaloid cells with follicular differentiation. It can present as a solitary lesion, multiple lesions, or an autosomal dominant inherited syndrome... -
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- Hypohidrotic Ectodermal Dysplasia
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Kim SK, Kim HK, Hwang SW
- KMID: 1678104
- Korean J Dermatol.
- 1980 Oct;18(5):471-477.
A case of hypohidrotic ectodermal dysplasia was seen at the Dermatological Clinic of Chosun Univeraity Hospital, with a classical symptom triad consisting of hypohidrosis to anhidroais, hypotrichosis and hypodontia, and... -
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- A Case of Keratitis, Ichthyosis and Deafness(KID) Syndrome
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Kim L, Lee DH
- KMID: 2335784
- J Korean Pediatr Soc.
- 2003 Nov;46(11):1135-1138.
KID syndrome was named after the initials of the major three symptoms of the disease; keratitis, ichthyosis, and deafness. The syndrome was first introduced by Dr. Burns in 1915 who... -
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- A Case of Hypohidrotic Ectodermal dysplasia
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Kim JH, Lee MH, Haw CR
- KMID: 2230803
- Korean J Dermatol.
- 1995 Oct;33(5):961-966.
Hypohidrotic ectodermali dysplasia is a rare and heterogenous genodermatosis that is characterzed by hypohidrosis, hyptrichosis, dental hypoplasia, and a characteristic facies. A 16-month-old male was evaluated for anodontia and anhidrosis... -
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- A Case of Anhidrotic Ectodermal Dysplasia with Atopic Dermatitis
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Yim YS, Kim GI, Park CW, Lee CH
- KMID: 2251092
- Korean J Dermatol.
- 2001 Feb;39(2):226-228.
Anhidrotic ectodermal dysplasia(AED) is a rare hereditary disorder characterized by hypohidrosis or anhidrosis, hypotrichosis, dental hypoplasia and characteristic facies. Additional less consistent symptoms include nail dystrophy, hyperkeratosis of the palms... -
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- A Case of Hypohidrotic Ectodermal Dysplasia
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Kim SH, Park SJ, Park KH, Yang JM, Lee ES
- KMID: 2086493
- Korean J Dermatol.
- 2001 Aug;39(8):955-958.
Hypohidrotic ectodermal dysplasia is a rare X-linked recessive disorder. It is characterized by the absence or hypoplasia of hair, teeth and sweat glands and by the characteristic facial features. A... -
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- A novel GLA mutation in a Korean boy with an early cardiac manifestation of Fabry disease
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Kwon S, Park JS, Jung JH, Hwang SK, Kim YH, Lee YJ
- KMID: 2435970
- J Genet Med.
- 2018 Jun;15(1):28-33.
- doi: 10.5734/JGM.2018.15.1.28
Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by the deficiency of α-galactosidase A. Patients with classical FD present acroparesthesia, hypohidrosis, cornea verticillata, disseminated angiokeratoma, and microalbuminuria... -
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- A Case of Stestocystoma Myltiplex
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Song JN, Lee JB, Jun SY, Kim JT
- KMID: 1664437
- Korean J Dermatol.
- 1974 Sep;12(3):203-205.
Steatocystoma multiplex is a relatively rare condition characterized by multiple, small, yellowish, cystic nodules 2 to 4mm in diameter locatcd princioally on the upper arms and the thighs. This has... -
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- A Case of anhidrotic Ectodermal Dysplasia
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Park CY, Kim HT, Choi SY, Kang YJ, Chung YC, Chang JK, Kim JW
- KMID: 2116019
- Korean J Dermatol.
- 1997 Oct;35(5):1005-1008.
Anhidrotic ectodermal dysplasia is inherited as an X linked recessive trait. This disor der is characterized by hypotrichosis, hypodontia and hypohidrosis. The diagnosis is often delayed until the first or... -
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- A Novel Frameshift Mutation of Galactosidase-alpha in Fabry Disease Restricted to Dermatologic Manifestations
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Kim DH, Kim SY, Im M, Lee Y, Seo YJ, Lee JH
- KMID: 2265979
- Ann Dermatol.
- 2013 Feb;25(1):95-98.
- doi: 10.5021/ad.2013.25.1.95
A 28-year-old Asian male was referred for dermatologic evaluation of diffuse bluish-red maculopapules in the lower trunk and genital regions. There was no family history, and with the exception of... -
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- A Case of Basaloid Follicular Hamartoma
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Go JW, Oh HE, Cho HK, Kang WH, Ro BI
- KMID: 2265403
- Ann Dermatol.
- 2010 May;22(2):229-231.
- doi: 10.5021/ad.2010.22.2.229
Basaloid follicular hamartoma (BFH), uncommon rare benign neoplasm connected to the adnexal structures, presents with multiple clinical manifestations that can develop into basal cell carcinoma. BFH may be congenital or... -
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- Congenital Insensitivity to Pain and Anhidrosis
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Shin JY, Kim SW, Roh SG, Lee NH, Yang KM
- KMID: 2167803
- Arch Plast Surg.
- 2016 Jan;43(1):95-97.
- doi: 10.5999/aps.2016.43.1.95
No abstract available. -
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