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Egyptian Journal of Medical Human Genetics [The]. 2013; 14 (3): 311-315
Dans Anglais | IMEMR | ID: emr-170467

Résumé

We report a 2 months old boy, the first in order of birth of non-consanguineous parents, with several typical features of oral-facial-digital syndrome type II [OFDS II] including cleft lip, high arched palate, retromicrognathia, preaxial polysyndactyly of hands and feet, duplication of thumb and hallux. Interestingly, the patient also had mesoaxial polydactyly of the left hand with extra metacarpal bones characteristic of OFDS. VI, however mentality and MRI brain were normal. This unusual association may suggest an additional subgroup of OFDSs or a variant of OFDS II due to variable gene expression or a transitional type between OFDS II and OFDS VI


Sujets)
Humains , Mâle , Expression des gènes , Imagerie par résonance magnétique , Encéphale/imagerie diagnostique
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