1.
Medical Journal of Mashad University of Medical Sciences. 2009; 52 (2): 119-122
in Persian
| IMEMR
| ID: emr-103603
ABSTRACT
Goltz syndrome [Focal Dermal Hypoplasia] is a rare syndrome results from developmental defects in tissues with meso-ectodermal origin such as skin, eyes, mouth and teeth, musculoskeletal and central nervous system. We report a 6 years old girl with FDH who had several features of skin, eyes and mouth involvement with multiple skeletal defects and absence of fibula which has not been reported previously