- The Right of Inheritance and Family Name of Embryo by Artificial Conception(54)
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Moon GJ
- KMID: 1683636
- J Korean Pediatr Soc.
- 1990 Oct;33(10):1461-1461.
No abstract available. -
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- Cleidocranial Dysostosis: One Case Report
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Yang JH, Jin GG, Seo H
- KMID: 2444548
- J Korean Orthop Assoc.
- 1988 Oct;23(5):1409-1412.
- doi: 10.4055/jkoa.1988.23.5.1409
The cleidocranial dysostosis is characterized by deficient formation of the clavicle, delayed and imperfect ossification of the cranium and less often involvement of other bones. The cleidocranial dysostosis is relatively... -
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- Two Cases of Congenital Ectodermal Defect
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Lee KY, Chung IH
- KMID: 1931002
- Korean J Dermatol.
- 1968 Jul;6(1):45-49.
Tow cases of congenital ectodermal defect in brothers aged 15 and 10 years were pesinted and the literature was reviewed. They had lack of sweating, sparseness of the hard hairs,... -
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- A Case of Harlequin Fetus
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Bak EH, Choi AS, Nicholson , Kwark YS, Lee JH
- KMID: 2208646
- J Korean Pediatr Soc.
- 1981 Oct;24(10):1009-1013.
The Harlequin fetus-ichthyosis fetalis-is known to be rare. Recently, we experienced a case of Harlequin fetus in stillborn infant due to autosomal recessive inheritance likely. A review of literature was... -
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- A Case of Epidermolytic Hyperkeratosis
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Kim MA, Yang SK, Kim JH
- KMID: 1664662
- Korean J Dermatol.
- 1976 Sep;14(3):283-287.
Epidermolytic Hyperkeratosis is a rare variant of ichthyosis, transmitted as autosomal dominant inheritance. A 2-year-old male baby, in whom no hereditary back ground was found, showed typical clinical and histopathological... -
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- Multiple occurance of gargoylism in a family
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Lee DH, Oh JS
- KMID: 2346053
- J Korean Radiol Soc.
- 1972 Dec;8(4):331-334.
- doi: 10.3348/jkrs.1972.8.4.331
Three patients with multiple occurance of Gargoylism in a family who were admitted to Kyungpook National University Hospital were observed. Two cases were siblings and another one was maternal relative... -
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- A Case of Dyschromatosis Symmetrica Hereditaria
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Ha DJ, Lee MH
- KMID: 1568863
- Korean J Dermatol.
- 2000 Oct;38(10):1411-1413.
Dyschromatosis symmetrica hereditaria(DSH), also known as reticulated acropigmentation of Dohi, is a rare pigmentary disorder that has autosomal dominant inheritance. Characteristic lesion includes a mixture of hyperpigmented and hypopigmented macules... -
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- A Case of Porokeratosis Plantaris Plamaris et Disseminata
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Park SH
- KMID: 2231578
- Korean J Dermatol.
- 1986 Oct;24(5):739-742.
Porokeratosis plantaris palmaris et disseminata is a rare variant of porokeratosis. A 37-year-old patient has been affected for about 2 years by mildly discornforting numerous, 1-3mm sized, keratotic lesions of... -
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- Five Cases of Hereditary Congenital Cataracts in One Family
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Kim DG, Yoon BJ
- KMID: 2204831
- J Korean Ophthalmol Soc.
- 1987 Oct;28(5):1101-1104.
The congenital cataract is the relatively common cause of the blindness in childhood, and its etiology is multiple but most of etiology is unknown. The inheritance is the largest single... -
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- A Case of Dyschromatosis Symmetrica Hereditaria
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Rhee TH, Ro YS
- KMID: 2303230
- Korean J Dermatol.
- 2000 Aug;38(8):1130-1132.
Dyschromatosis symmetrica hereditaria (DSH) is characterized by a symmetrical distribution of hyperpigmented and hypopigmented macules on the extremities, especially over the dorsa of the hands and feet. The pattern of... -
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- A Case of Adynamia Episodica Hereditaria
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Hu K, Choi IS, Kim KH
- KMID: 1957588
- J Korean Neurol Assoc.
- 1983 Jun;1(1):101-105.
Four members of a family suffering from frequent attacks of flaccid paralysis with asymptomatic myotonia were evaluated. There was an autosomal dominant pattern of inheritance and their earliest symptoms were... -
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- Two Cases Report of Cleidocranial Dysostosis
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Kim KH, Choi IY, Kim SJ, Park SB
- KMID: 2450803
- J Korean Orthop Assoc.
- 1981 Jun;16(2):497-502.
- doi: 10.4055/jkoa.1981.16.2.497
The cleidocranial dysostosis is relatively rare congenital and familial disorder with autosomal dominant inheritance. After the first report of a case of this was that of Cutter in 1870, which... -
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- Dyschromatosis Universalis Hereditaria
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Shin HK, Han EH, Kwon KS, Chung TA
- KMID: 1681231
- Korean J Dermatol.
- 1994 Jun;32(3):493-497.
Dyschromatosis universalis hereditaria is a rare pigmentary disorder characterized by widespread mothed hyperpigmentation and hypopigmentation. We report a 40-year-old male patient with numerous hyperpigmenter, and hypopigmented macules all over the... -
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- Spondylometaphyseal Dyslpasia
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Kim KS, Lim BK, Kim DH, Lee BI, Han DY, Oh KK
- KMID: 2103972
- J Korean Pediatr Soc.
- 1980 Sep;23(9):748-752.
There sibs with identical features of short-limbed dwarfism, a normal skull and face and normal intelligence are described. On the basis of the radiological and clinical characteristics, the condition must... -
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- A Case of Type 2 Waardenburg Syndrome with Open angle Glaucoma
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Lee OY, Choi YJ, Jung NH
- KMID: 2205704
- J Korean Ophthalmol Soc.
- 1999 Dec;40(12):3532-3535.
Waardenburg syndrome is a very rare auditory-pigment syndrome with autosomal dominant inheritance. In his first report in 1951, Waardenburg characterized this syndrome as dystopia canthorum, a high broad nasal bridge,... -
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- Disseminated Superficial Actinic Porokeratosis ( DSAP ): Case Report and Review of Literatures
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Juhn SY, Suh JK, Lee YS
- KMID: 2231833
- Korean J Dermatol.
- 1971 Jan;9(1):53-56.
A case of disseminated superficial actinic poroLeratosis affecting 47 years old, house wife, who has been suffering from multiple dark-brownish keratotic papules on the sun-light exposed parts especially face, forearm... -
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- Recognition of Advance Directives by Advanced Cancer Patients and Medical Doctors in Hospice Care Ward
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Sun DS, Chun YJ, Lee JH, Gil SH, Shim BY, Lee OK, Jung IS, Kim HK
- KMID: 1464991
- Korean J Hosp Palliat Care.
- 2009 Mar;12(1):20-26.
PURPOSE: We undertook this study to find out the recognitions of terminal cancer patients and doctors about advance directives (ADs), of how they would do in non-response medical conditions and... -
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- A Case of Pili Torti
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Park JJ, Chung H, Chung BS
- KMID: 2230810
- Korean J Dermatol.
- 1995 Oct;33(5):998-1001.
In pili torti, the affected Eair shaft is flattened and twisted through 180 degrees on its own axis. The involved hairs are dry, thin, brittle, and break off easily. Congenital... -
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- A Case of Reticulated Acropigmentation of Dohi
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Lee GY, Choi YW, Choi HY, Myung KB
- KMID: 2303186
- Korean J Dermatol.
- 2001 Jan;39(1):71-74.
Reticulated acropigmentation of Dohi(RAD) is a dyschromic disorder that has an autosomal dominant pattern of inheritance. RAD is characterized by the intermingled hyperpigmented and hypopigmented macules and its bilaterally symmetrical... -
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- A Case of Brachyonychia Showing Typical Autosomal Dominant Pattern of Inheritance
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Kim JH, Ro YS
- KMID: 2250800
- Korean J Dermatol.
- 2002 Jul;40(7):855-856.
Brachyonychia or racquet nail is a condition that the width of the nail plate is greater than the length. It may occur in isolation or in association with shortening of... -
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