Goltz Syndrome Associated with Omphalocele
Journal of the Korean Surgical Society
;
: 238-240, 2011.
Article
in Korean
| WPRIM
| ID: wpr-186550
ABSTRACT
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 than 200 cases of Goltz syndrome were reported in the world literature, and 5 cases have been reported in Korea since 1994. There were few descriptions in the literature regarding surgical experience in Goltz syndrome. We report a female neonate born with omphalocele associated with Goltz syndrome that included typical cutaneous manifestations and a lobster-claw defect of the left foot. Omphalocele was successfully closed by staged reduction without any wound problems.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Wounds and Injuries
/
Focal Dermal Hypoplasia
/
Ectoderm
/
Foot
/
Hernia, Umbilical
/
Korea
/
Mesoderm
/
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Limits:
Female
/
Humans
/
Infant, Newborn
Country/Region as subject:
Asia
Language:
Korean
Journal:
Journal of the Korean Surgical Society
Year:
2011
Type:
Article
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