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Focal dermal hypoplasia (Goltz syndrome): case reports

dc.contributor.authorDerks, B.en_ZA
dc.contributor.authorGericke, G. S.en_ZA
dc.contributor.authorLouw, M.en_ZA
dc.date.accessioned2011-03-18T14:57:50Z
dc.date.available2011-03-18T14:57:50Z
dc.date.issued1978
dc.identifier.citationDerks, B., Gericke, G. S. & Louw, M. 1978. Focal dermal hypoplasia (Goltz syndrome): case reports. South African Medical Journal, 54(1):27-29
dc.identifier.issn2078-5135 (online)
dc.identifier.issn0256-9574 (print)
dc.identifier.urihttp://hdl.handle.net/10019.1/7683
dc.descriptionCITATION: Derks, B., Gericke, G. S. & Louw, M. 1978. Focal dermal hypoplasia (Goltz syndrome): case reports. South African Medical Journal, 54(1):27-29.
dc.descriptionThe original publication is available at http://www.samj.org.za
dc.description.abstractTwo children, both with physical stigmata of Goltz syndrome, are described. Accurate diagnosis of congenital defects in the newborn allows optimal planning of surgical treatment and more accurate prognosis and genetic counselling.
dc.language.isoenen_ZA
dc.publisherHealth & Medical Publishing Group
dc.subjectEctodermal dysplasia
dc.titleFocal dermal hypoplasia (Goltz syndrome): case reportsen_ZA
dc.typeArticle
dc.description.versionPublisher’s version
dc.rights.holderSouth African Medical Journal


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