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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


Subject(s)
Humans , Female , Fibula/abnormalities , Skin/pathology , Eye/pathology , Mouth/pathology , Musculoskeletal Abnormalities
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