- A Case of Hereditary Hypotrichosis (Marie Unna Type)
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Cho JH, Kim MY, Kim OH, Kim YT
- KMID: 2302777
- Korean J Dermatol.
- 2004 Nov;42(11):1495-1498.
We report a patient suffering from Marie Unna's hypotrichosis. A 24-year-old man presented with a progressive hair loss. Since puberty, he had experienced a loss of hair on the scalp,... -
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- Hereditary Hypotrichosis ( Marie Unna Type )
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Kim YG, Lee ES, Lee KH
- KMID: 2231289
- Korean J Dermatol.
- 1990 Feb;28(1):112-117.
We report a family suffering from Marie Unnas hypotrichosis (8 members affected in 4 generations). At birth they had normal hairs, subsequently loss of hair on the scalp, eyebrow and... -
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- Non-familial Generalized Hypotrichosis Simplex
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Namkoong S, Kim JY, Gye J, Chung J, Hong SP, Kim MH, Park BC
- KMID: 1451731
- Korean J Dermatol.
- 2011 Oct;49(10):940-942.
Hypotrichosis simplex is a descriptive term of hair loss without other ectodermal or systemic abnormalities. Hypotrichosis simplex with non-familial and generalized types has been seldom reported. A 30-year-old man visited... -
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- Hypomelia-Hypotrichosis-Facial Hemangioma Syndrome
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Lew W, Kim DK, Cho NJ, Kim YC, Park HW
- KMID: 2361370
- Ann Dermatol.
- 1995 Oct;7(4):358-360.
- doi: 10.5021/ad.1995.7.4.358
We report a mild variant of hypomelia-hypotrichosis-facial hemangioma syndrome in a 3 month-old female. The patient showed major features of the previously reported cases including flexion deformities of both upper... -
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- Non-Familial Congenital Hypotrichosis: Report of 11 Cases
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Eun HC, Kwon OS, Kim SD, Suh DH
- KMID: 2163941
- Ann Dermatol.
- 2000 Mar;12(1):26-32.
- doi: 10.5021/ad.2000.12.1.26
BACKGROUND: Congenital hypotrichosis is a non-specific, descriptive term for structural abnormalities of hairs showing variable clinical features. We recently have encountered a group of eleven patients exhibiting abnormal hairs showing... -
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- A Case of Oculodentodigital Dysplasia
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Kim DK, Cho DS, Chang WU, Park SY
- KMID: 2107282
- J Korean Ophthalmol Soc.
- 1979 Jun;20(2):193-197.
A case, 21 years old male, of Oculodentodigital dysplasia characterized with microphthalmia, micrccornea, parrot beak nose, dental anormalies, hypotrichosis and syndactyly. A brief review of literature is described. -
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- Dermtosurgical Treatment of Hypotrichosis of Pubis and Atrichia Pubis with the Additive Effect of Testosterone Cream
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Suh DH, Lee Y
- KMID: 1977856
- Korean J Dermatol.
- 2003 Dec;41(12):1627-1632.
BACKGROUND: The incidence of hypotrichosis of pubis and atrichia pubis is relatively higher in oriental countries including Korea. OBJECTIVE: The aim of this study was to develop a treatment method... -
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- A Case of Hypotrichosis Simplex of the Scalp
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Park CO, Oh SW, Lee WS, Kim SC
- KMID: 1891833
- Korean J Dermatol.
- 2006 Feb;44(2):212-215.
We report a sporadic case of hypotrichosis simplex of the scalp, a rare genotrichosis, characterized by sparse or absent scalp hair with no structural defect of the hair shaft, in... -
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- A Case of Hallermann-Streiff Syndrome
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Shim WS, Kim KR
- KMID: 1948431
- J Korean Ophthalmol Soc.
- 1976 Sep;17(3):297-301.
Twenty years old Korean male patient with Hallermann-Streiff syndrome who developed glaucoma is reported. The clinical features are dyscephalia with mandibulo-oculo-facial malformation, bilateral congenital cataract, dental anomalies, hypotrichosis, microphthalmia, nanism... -
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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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- A Case of Hallermann-Streiff Syndrome
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Koo BS, Rhee SU, Kim JH
- KMID: 1948602
- J Korean Ophthalmol Soc.
- 1967 Jun;8(1):55-60.
A case of Hallermann-Streiff syndrome characterized by dyscephalia with bird face, dental anomalies, proportionate nanism, hypotrichosis or atrichosis, atrophy of the skin, bilateral microphthalmia and presumed congenital cataract was reported.... -
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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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- 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 Hallermann Streiff Syndrome
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Lee HB, Kim JH
- KMID: 2336382
- J Korean Ophthalmol Soc.
- 1978 Dec;19(4):455-459.
A Case, 17 yrs, old male, of Hallermann Streiff syndrome characterized by dyscephalia with bird face, dental anormalies, Nanism, hypotrichosis, atrophy of the skin, bilateral microphthalmos, and congenital cataracts has... -
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- Two Cases of Hallermann-Streiff Syndrome Diagnosed in Early Neonatal Period
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Choi YE, Choi JS, Kim YN, Song ES, Choi YY
- KMID: 2188354
- J Korean Soc Neonatol.
- 2012 Aug;19(3):146-153.
- doi: 10.5385/jksn.2012.19.3.146
Hallermann-Streiff syndrome is a very rare congenital disorder, which is primarily characterized by the head and face abnormalities. Approximately 180 cases have been reported worldwide, including 8 cases in Korea... -
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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 case of Hallermann-Streiff syndrome with aphakia
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Lee MC, Choi IJ, Jung JW
- KMID: 2280302
- Korean J Pediatr.
- 2008 Jun;51(6):646-649.
- doi: 10.3345/kjp.2008.51.6.646
Hallermann-Streiff syndrome is a rare disease. Approximately 150 cases have been reported, including 6 cases in Korea. The authors experienced a case of Hallermann-Streiff syndrome in a 6-year-old female with... -
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- A Case of Hellermann-Streiff Syndrome
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Ryoo MH, Kim SS, Yi KP
- KMID: 2107654
- J Korean Ophthalmol Soc.
- 1990 Jun;31(6):831-836.
Hallermann-Streiff Syndrome is a rare congenital anomaly characterized by dyscephalia, dental anomalies, hypotrichosis, congenital cataract, bilateral microphthalmia and has characteristic feature of bird face due to marked mandibular hypoplasia and... -
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- A Case of Hereditary Anhidrotic Ectodermal Dysplasia
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Lee JW, Jung JK, Bang JG, Rho JS, Park JH
- KMID: 2208490
- J Korean Pediatr Soc.
- 1994 Oct;37(10):1453-1456.
Hereditary anhidrotic ectodermal dysplasia is a rare condition characterized by underdeveloped ectodermal structure including the skin, teeth or skin appendages. The patient has characteristic feature of anhidrosis, hypotrichosis and defective... -
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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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