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3 rezultatov
[Malformation-retardation syndrome with lobster claws, coloboma of the iris, renal agenesia and ventricular septal defect].
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Three cases of focal dermal hypoplasia (Goltz syndrome).
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Focal dermal hypoplasia or Goltz syndrome is a rare genodermatosis, characterized by multiple abnormalities of ectodermal and mesodermal origin. It is found predominantly in females and is characterized by hypoplasia of skin and papillomas. Three cases of focal dermal hypoplasia in infancy with
Goltz syndrome (focal dermal hypoplasia) with unilateral ocular, cutaneous and skeletal features: case report.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
BACKGROUND
Goltz syndrome or focal dermal hypoplasia (FDH) is an uncommon multisystem disorder. Herein, we report a typical case of FDH with unilateral ocular, cutaneous and skeletal features.
METHODS
a 4-year-old girl presented with microphthalmos and iris coloboma of the left eye, facial
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