[Goltz syndrome with absence of fibula]
Medical Journal of Mashad University of Medical Sciences. 2009; 52 (2): 119-122
Dans Persan
| 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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Indice:
Méditerranée orientale
Sujet Principal:
Peau
/
Oeil
/
Fibula
/
Bouche
/
Malformations de l'appareil locomoteur
Type d'étude:
Enquête cas-témoins / Études cas/témoins
Limites du sujet:
Femelle
/
Humains
langue:
Persan
Texte intégral:
Med. J. Mashad Univ. Med. Sci.
Année:
2009
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