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Case Report
A Case of Incontinentia Pigmenti with Developmental Brain Malformation
Suk Ho Kang, Soon Kim, Seung Hee Jung, Sang Geel Lee
Clin Exp Pediatr. 2002;45(4):535-539.   Published online April 15, 2002
Incontinentia pigmenti is a rare neurocutaneous syndrome characterized by vesiculobullous skin disease in neonates and infants, a noninfectious disease that should be distinguished from infectious diseases with the neonatal seizure or encephalopathy. This disease is X-linked dominant with Xq28 region abnormalities and often associated with developmental defects of the ocular, skeletal, dental, and central nervous system. Central nervous system involvement...
A Case of Incontinentia Pigmenti
Soo Am Chung, Won Rae Kim, Hyung Kun Nam, Jin Sam No, Jung Hee Park
Clin Exp Pediatr. 1993;36(3):428-433.   Published online March 15, 1993
Incontinentia pigmenti (Bloch-Sulzberger syndrome)is a genetic disease of the skin with generalized ectodermal and mesodermal dysplasia. Skin lesions are uually present at birth or shortly after in the form of eythermatous eruptions with linear vesiculations. The final stage is characterised by irregular macular streaks of brown to slate-grey pigmentation. We experienced five cases of incontinentia pigmenti maternal female relative of a...
A Case of Incontinentia Pigmenti
Soo Young Kweon, Hyun Joo Choi, Gyung Hee Kim
Clin Exp Pediatr. 1992;35(3):417-421.   Published online March 15, 1992
Incontinentia Pigmenti is an uncommon genodermatosis that usually affects female infants. The dermatosis may be only a part of more generalized disorder which may affect with great variability the teeth, the eyes, the bones or central nervous system, or may be associated with other malformations or developmental disturbances. We experienced a case of Incontinentia Pigmenti associated with defect of a eye...
Original Article
A case of incontinentia pigmenti.
Kwang Ik Song, Hyo Jeong Kim, Jin Bok Hwang, Chang Ho Han, Hye Li Chung, Young Dae Kwon
Clin Exp Pediatr. 1991;34(10):1446-1451.   Published online October 31, 1991
A case of incontinentia pigmenti, Bloch-Sulzberger type, without any developmental defect has been presented with the review of related literatures. The patient was a 4 day-old female infant with irregular, grouped vesicobullous lesions on the whole body, especially on the trunk and extremities since birth. No familial traits was noted. Diagnosis was made by the charateristic clinical, labaratory and histopathologic findings.
A Case of Incontinetia Pigmenti Associated with Convulsions.
Young Ok Suh, Gyun Woo Lee, Un Ki Yoon, Ji Sub Oh, Kee Suck Suh, Sang Tae Kim
Clin Exp Pediatr. 1988;31(5):641-647.   Published online May 31, 1988
Incontinentia pigmenti is a complex hereditary syndrome in which vesicular, verrucous and pigmented cutaneous lesions are associated with developmental defects of the eye, skeletal system and central nervous system. A case of incontinentia pigmenti associated with convulsions, Block-Sulzberger type, is presented with a review of related literatures. The patient was a 40 day-old female infant with convulsions and verrucous, dark brown pigmented lesions on the trunk...
Case Report
A case of Incontinentia Pigmenti.
Wan Seob kim, Yong Woo Choi, Myung Ho Lee, Chul Wan Lim
Clin Exp Pediatr. 1985;28(9):940-944.   Published online September 30, 1985
A case of incontinentia pigmenti with CNS involvement was presented. And literatures have been reviewed. The patient was a 7 month-old female had been affected with numerous dark brownishinear streaks, irregular macules, and splashes of brown to slate gray pigmentation on the entire body, especially both trunk, axillary, and extremity. The chief complaint was severe vomiting and comatous mental state for...
A case of Incontinentia Pigmenti.
Hyun Mo Koo, Chun Dong Kim, Byung Ryul Choi, Han Gu Moon, Yong Hoon Park, Jin Gon Jun, Jeong Ok Hah
Clin Exp Pediatr. 1985;28(4):396-399.   Published online April 30, 1985
A case of Incontinentia pigmenti, Bloch-Sulzberger type, is presented with the review of related literatures. One month old female infant was admitted with irregular, grouped vesicobullous lesion on the whole body especially on the trunk and extremities which have been persistent since birth. No familial traits were noted. Diagnosis was made by the characteristic clinical and laboratory and histopathologic：findings