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Case Report

Won Rae Kim, Hyang Joo Kim, Ghee Young Jung, Jin Gun Bang, Du Bong Lee, Jung Hee Park

Clin Exp Pediatr. 1994;37(7):994-998. Published online July 15, 1994

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, ophthalmological and other abnormalities. We experienced a case of Goltz syndrome. An one day old female newborn had focal atrophic and telangiectatic skin lesions, microphthalmia, syndactyly and urinary tract abnormality. The finding...

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