- Focal Dermal Hypoplasia Associated with Ichthyosis
-
Cho MK, Kim YK, Lee JS, Whang KU, Jung SH
- KMID: 2361732
- Ann Dermatol.
- 1993 Jan;5(1):34-37.
- doi: 10.5021/ad.1993.5.1.34
We report a case of focal dermal hypoplasia associated with ichthyosis in an 18-year-old Korean female. The patient showed a yellowish atrophic patch on the left side of her abdomen,... -
- CITED
-
- Close
- SHARE
-
- Close
- Almost Unilateral Focal Dermal Hypoplasia
-
Lee S, Choe SJ, Ahn SK
- KMID: 2368035
- Ann Dermatol.
- 2017 Feb;29(1):91-94.
- doi: 10.5021/ad.2017.29.1.91
Focal dermal hypoplasia, caused by mutations in PORCN, is an X-linked ectodermal dysplasia, also known as Goltz syndrome. Only seven cases of unilateral or almost unilateral focal dermal hypoplasia have... -
- CITED
-
- Close
- SHARE
-
- Close
- A case of focal dermal hypoplasia
-
Koh MO, Jeon BK, Park SD
- KMID: 1693132
- Korean J Dermatol.
- 1992 Apr;30(2):262-266.
Focal dermal hypoplasia (Goltz syndrome) is a rare genetic mesoectodermal disorder characterized by variable multisystem defects, including anomalies of the skin, skeleton, teeth and eyes. A 22-year-old female patient presented... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Goltz Syndrome
-
Cho SW, Lew W, Choi EH, Lee SH, Lee SN, Lee SH
- KMID: 2362029
- Ann Dermatol.
- 1991 Jan;3(1):84-89.
- doi: 10.5021/ad.1991.3.1.84
Goltz syndrome, also known as focal dermal hypoplasia syndrome, is a rare congenital mesoectodermal disorder. Two cases, which we experienced, showed erythematous, tan skin rashes and atrophic scars on the... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Goltz Syndrome
-
Bae YI, Yun SJ, Lee JB, Kim SJ, Won YH, Lee SC
- KMID: 2087924
- Korean J Dermatol.
- 2008 Jan;46(1):122-125.
Goltz syndrome or focal dermal hypoplasia, is a rare genodermatosis, characterized by multiple abnormalities of mesodemal and ectodermal organs. Cutaneous manifestations include linear or cribriform atrophied patches with telangiectasia following... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Goltz Syndrome
-
Kim WR, Kim HJ, Jung GY, Bang JG, Lee DB, Park JH
- KMID: 1879424
- J Korean Pediatr Soc.
- 1994 Jul;37(7):994-998.
Goltz syndrome is known as a rare mesoectodermal hereditary disease, characterized by focal dermal atrophies with hernias of adipose tissue and also associated with a multitude of possible skeletal, dental,... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Focal Dermal Hypoplasia
-
Kim CD, Ryoo YW, Lee KS
- KMID: 2250956
- Korean J Dermatol.
- 2001 Dec;39(12):1411-1414.
Focal dermal hypoplasia or Goltz syndrome is a rare genetic mesodermal and ectodermal disorder characterized by variable multisystem defects, including anomalies of the skin, skeleton, teeth and eyes. The disorder... -
- CITED
-
- Close
- SHARE
-
- Close
- Goltz Syndrome Associated with Omphalocele
-
Lee HW, Byun CS, Hong J
- KMID: 1963589
- J Korean Surg Soc.
- 2011 Mar;80(3):238-240.
- doi: 10.4174/jkss.2011.80.3.238
Goltz syndrome is a rare congenital disorder characterized by ectodermal and mesodermal dysplasia with multisystem defects. It was first reported in 1962 by Goltz as a focal dermal hypoplasia. More... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Goltz Syndrome
-
Lee DH, Park CH, Park JM, Park SB, Kim HS, Ryoo YW, Lee KS, Lee HJ
- KMID: 1606829
- J Korean Pediatr Soc.
- 2003 Jun;46(6):606-609.
Goltz syndrome(focal dermal hypoplasia) is a rare disorder characterized by ectodermal and mesodermal dysplasia described in 1962 by Goltz. In Korea, one case of Goltz syndrome was reported in 1994.... -
- CITED
-
- Close
- SHARE
-
- Close
