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Prog. diagn. trat. prenat. (Ed. impr.) ; 16(4): 182-185, 2004. ilus
Article in Portuguese | IBECS | ID: ibc-152054

ABSTRACT

Os autores apresentam um caso clínico de Síndrome de Grebe, urna doenca rara, autossómica recessiva, caracterizada por encurtamento e dismofogenese severos dos membros e efectuara urna breve revisáo bibliográfica sobre esta patología (AU)


Los autores presentan un caso clínico de síndrome de Grebe, una patología rara, autosómica recesiva, caracterizada por acortamiento y dismorfogénesis severos de los miembros y efectúan una breve revisión bibliográfica sobre esta patología (AU)


The authors report a case of Grebe syndrome, a rare, autosomal recessive disorder, characterized by severe limb shortening and dysmorphogenesis, and make a brief bibliographic review about this disease (AU


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Weill-Marchesani Syndrome/complications , Weill-Marchesani Syndrome/genetics , Chromosome Disorders/genetics , Uterine Cervical Dysplasia/metabolism , Uterine Cervical Dysplasia/pathology , Upper Extremity/injuries , Weill-Marchesani Syndrome/metabolism , Weill-Marchesani Syndrome/pathology , Chromosome Disorders/pathology , Uterine Cervical Dysplasia/complications , Uterine Cervical Dysplasia/genetics , Upper Extremity/pathology
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