[Goltz syndrome with absence of fibula]
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
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Skin
/
Eye
/
Fibula
/
Mouth
/
Musculoskeletal Abnormalities
Type of study:
Case report
Limits:
Female
/
Humans
Language:
Persian
Journal:
Med. J. Mashad Univ. Med. Sci.
Year:
2009
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