[Goltz syndrome with absence of fibula]
Medical Journal of Mashad University of Medical Sciences. 2009; 52 (2): 119-122
em Persa
| 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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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Pele
/
Olho
/
Fíbula
/
Boca
/
Anormalidades Musculoesqueléticas
Tipo de estudo:
Relato de Casos
Limite:
Feminino
/
Humanos
Idioma:
Persa
Revista:
Med. J. Mashad Univ. Med. Sci.
Ano de publicação:
2009
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