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Original Article

A case of hypomelanosis of Ito accompanying ureteral duplication and hypomelanotic scalp hair.

Dong Woo Son, Beom Soo Park, Heon Seok Han, Hae Il Jung, Yong Choi, Hyung Ro Moon, Seon Hoon Kim, Hwang Choi

Clin Exp Pediatr. 1991;34(2):281-286. Published online February 28, 1991

Hypomelanosis of Ito (incontinentia pigmenti achromians) is a cutaneous abnormality consisting of bizarre, whorly, linear, or patchy hypopigmentation over variable portion of body surface. Multiple assocaited defects in other systems occur in three quarters of the affected individuals. Most common- ly, the central nervous system, eye, and musculoskeletal structures are involved. It is suggested that the cutaneous abnormality, which is often detectable at birth...

A Clinical Study of Ureteral Duplication : Review of 90 Cases.

Jun Chul Choi, Jae Seung Lee, Ho Yung Lee, Dae Suk Han, Hyung Ki Choi, Jin Moo Lee, Jin Suck Suh

Clin Exp Pediatr. 1986;29(2):170-177. Published online February 28, 1986

Ureteral duplication is one of the most common congenital malformations of the urinary tract. Incomplete duplication rarely causes clinical problems, but complete duplication often accompanies complications of a varying degree. We herein analyzed, retrospectively, 90 cases with ureteral duplication who were admitted to Yonsei University Severance Hospital during 13.5 years. There were 28 cases under age of 15 years. Thirty-four cases...

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