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A CASE OF FOCAL DERMAL HYPOPLASIA (GOLTZ SYNDROME) WITH SOME NEW ASPECTS
Author(s) -
BEGANOVIĆ N.,
LOMMEN E. J. P.
Publication year - 1977
Publication title -
acta pædiatrica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 115
eISSN - 1651-2227
pISSN - 0803-5253
DOI - 10.1111/j.1651-2227.1977.tb07844.x
Subject(s) - medicine , hypoplasia , dermatology , pediatrics , anatomy
Beganović, N. and Lommcn, E. J. P. (Paediatric Department, St. Josephziekenhuis, Eindhoven, the Netherlands). A case of focal dermal hypoplasia (Goltz syndrome), with some new aspects. Acta Paediatr Scand, 66:255, 1977.—A case of Focal Dermal Hypoplasia (Goltz syndrome), diagnosed at birth, is reported. Some findings not formerly described (hemimelia, schizis of the palatum molle and the absence of one umbilical artery) are reported. Normal findings in chromosome studies with banding techniques are discussed.