- A Case of Hereditary Anhidrotic Ectodermal Dysplasia
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Lee JB, Houh W
- KMID: 1664289
- Korean J Dermatol.
- 1973 Oct;11(2):69-72.
A case of hereditary anhidrotic ectodermal dysplasia associated with atopic dermatitis in 16 month old male is reported. He has been suffered from multiple symptoms of anhidrosis, hypotrichosis, anodontia and... -
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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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- Interdisciplinary treatment for ectodermal dysplasia
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Kim JH, Hoe YK, Oh JK
- KMID: 1576271
- Korean J Orthod.
- 2000 Dec;30(6):739-745.
Ectodermal dysplasia is a hereditary disease characterized by a congenital dysplasia of one or more ectodermal structures. Characteristic manifestations include scanty hair and eyebrows, pigmented and hyperkeratinized skin around the... -
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- Dento-maxillofacial abnormalities caused by radiotherapy and chemotherapy
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Park CW, Hwang EH, Lee SR
- KMID: 2033988
- Korean J Oral Maxillofac Radiol.
- 2000 Dec;30(4):287-292.
A case of dento-maxillofacial abnormality involving a 10-year-old male patient with a history of esthesioneuroblastoma is presented. This patient had been treated with 54 Gy (60)Co-gamma-radiation to the nasal cavity... -
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- A Case of Anhidrotic Ectodermal Dysplasia with Atrophic Rhinitis
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Lee YS, Kim JE, Wee SJ, Lim SK
- KMID: 1977242
- Korean J Otolaryngol-Head Neck Surg.
- 2007 Feb;50(2):174-177.
Anhidrotic ectodermal dysplasia is a rare genetic disorder characterized by absence or diminished numbers of structures derived from the ectoderm, and it is reported to be inherited as an x-linked... -
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- Analysis of Oral State of Hansen's Patients and Denture fabrication for Pre-Prothodontic Oro-maxillofacial minor surgury
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Oh DC
- KMID: 2036963
- Korean Lepr Bull.
- 2007 Jun;40(1):31-49.
The purposes of this study were to investigate the oral health care conditions of patients who have Leprous disease, which is an infectious disease(Dental caries: DMF rate and DMFT rate,... -
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- A morphometric analysis of maxillary central incisor on the basis of facial appearance in Korea
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Ku JE, Yang HS, Yun KD
- KMID: 2284778
- J Adv Prosthodont.
- 2012 Feb;4(1):13-17.
- doi: 10.4047/jap.2012.4.1.13
PURPOSE: We aimed to identify a more esthetic width-to-length ratio by analyzing maxillary central incisor of Korean adult population. Information regarding tooth ratio in the Korean population may be useful... -
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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 of Anhidrotic Ectodermal Dysplasia with Atopic Dermatitis in Siblings
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Kim HS, Oh CW
- KMID: 2359800
- Ann Dermatol.
- 1998 Apr;10(2):91-96.
- doi: 10.5021/ad.1998.10.2.91
Anhidrotic ectodermal dysplasia (AED) is characterized by a well-known tetrad of anhidrosis, hypotrichosis, hypodontia, and typical facies with a wide constellation of developmental defects of tissues derived from the ectoderm.... -
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- Prosthetic management of a growing patient with Russell-Silver syndrome: a clinical report
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Kim K, Noh K, Paek J, Kwon KR, Pae A
- KMID: 2083885
- J Adv Prosthodont.
- 2015 Oct;7(5):406-410.
- doi: 10.4047/jap.2015.7.5.406
Russell-Silver syndrome (RSS) is a congenital disease characterized by short stature due to growth hormone deficiency, physical asymmetry, inverted triangular face, micrognathia, prominent forehead, and hypodontia. This case report presents... -
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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 Coffin-Lowry syndrome
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Shin JE, Seo ES, Lee DH
- KMID: 2288523
- J Genet Med.
- 2007 Dec;4(2):196-199.
Coffin-Lowry syndrome (CLS) is a rare X-linked hereditary disorder characterized by moderate to severe mental retardation, facial dysmorphism, tapering fingers, and skeletal deformity. A 12-month-old boy was referred to our... -
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- Ankyloblepharon, Ectodermal Defects, and Cleft Lip and Palate Syndrome Associated with TP63 Gene Mutation
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Song KH
- KMID: 2088187
- Korean J Dermatol.
- 2011 Mar;49(3):274-278.
Ankyloblepharon, Ectodermal defects, and Cleft lip and palate (AEC) syndrome, also known as Hay-Wells syndrome, is a rare form of ectodermal dysplasia initially described by Hay and Wells in 1976.... -
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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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- Van der Woude syndrome presenting as a single median lower lip pit with associated dental, orofacial and limb deformities: a rare case report
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Richardson S, Khandeparker RV
- KMID: 2391358
- J Korean Assoc Oral Maxillofac Surg.
- 2017 Aug;43(4):267-271.
- doi: 10.5125/jkaoms.2017.43.4.267
Although it is a rare developmental malformation, van der Woude syndrome is the most common form of syndromic orofacial clefting, accounting for approximately 2% of all cleft cases. The lower... -
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- Alveolar ridge expansion-assisted orthodontic space closure in the mandibular posterior region
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Ozer M, Akdeniz BS, Sumer M
- KMID: 2273424
- Korean J Orthod.
- 2013 Dec;43(6):302-310.
- doi: 10.4041/kjod.2013.43.6.302
Orthodontic closure of old, edentulous spaces in the mandibular posterior region is a major challenge. In this report, we describe a method of orthodontic closure of edentulous spaces in the... -
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- Full mouth implant rehabilitation of a patient with ectodermal dysplasia after orthognathic surgery, sinus and ridge augmentation: a clinical report
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Bayat M, Khobyari M, Dalband M, Momen-Heravi F
- KMID: 1975084
- J Adv Prosthodont.
- 2011 Jun;3(2):96-100.
- doi: 10.4047/jap.2011.3.2.96
An 18-year-old male presented severe hypodontia due to hypohidrotic ectodermal dysplasia was treated with Le Fort I maxillary osteotomy with simultaneous sinus floor augmentation using the mixture of cortical autogenous... -
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- Kabuki syndrome with phonetic and dental problem: A case report
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Lee JS, Ko SO, Leem DH, Baek JA, Shin HK
- KMID: 1814536
- J Korean Assoc Oral Maxillofac Surg.
- 2007 Dec;33(6):681-683.
Kabuki (Niikawa-Kuroki) syndrome was first reported by Niikawa et al(1981). The faces of the patients are similar to the make-up of traditional Japanese Kabuki actors: long palpebral fissures, an ectropium... -
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- A Case Report of Van der Woude Syndrome
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Lee SC, Kang YS, Lee MJ, Lee CK, Yang JY
- KMID: 2329685
- J Korean Cleft Palate-Craniofac Assoc.
- 2000 Oct;1(1):115-117.
Van der Woude syndrome is a rare developmental malformation characterized by pits in the lower lip, usually bilateral and located on either side of the midline. Van der Woude syndrome... -
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- Hypohidrotic Ectodermal Dysplasia Associated with Glucose-6-Phosphate Dehydrogenase Deficiency
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Ermertcan , Yasar A, Kayhan TC, Gulen H, Ertan P
- KMID: 2156740
- Ann Dermatol.
- 2011 Sep;23(Suppl 1):S8-S10.
- doi: 10.5021/ad.2011.23.S1.S8
Hypohidrotic ectodermal dysplasia (HED) is a syndrome characterized by hypodontia, hypotrichosis, and partial or total ecrine sweat gland deficiency. The most prevalent form of HED is inherited as an X... -
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