AbstractWe report a 2months 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
AbstractWe report a 4.5year old Egyptian male child, fourth in the order of birth of healthy remote ...
Oral-facial-digital syndromes (OFDS) represent a heterogeneous group of rare developmental disorders...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...
We report a 2 months old boy, the first in order of birth of non-consanguineous parents, with sever...
AbstractWe report a 2months old boy, the first in order of birth of non-consanguineous parents, with...
AbstractWe report a 4month old male infant, the first in order of birth of healthy first cousin cons...
Oral-facial-digital syndrome (OFDS) is a group of disorders characterized by oral cavity malformatio...
The oral-facial-digital syndromes (OFD) are part of a great number of genetic disorders. They are cl...
We report the case of a 2.5 year old female, 2nd in order of birth of 1st cousin consanguineous marr...
Oral-facial-digital syndrome as heterogeneous developmental conditions is characterized by abnormali...
This is the final version. Available on open access from Tehran University of Medical Sciences via t...
Oro-facial-digital syndrome (OFD) is a rare congenital disorder. Its incidence in the general popula...
AbstractBackgroundMiller syndrome is one of the acrofacial dysostosis syndromes, which are character...
Copyright © 2014 Meltem Ozdemir-Karatas et al. This is an open access article distributed under the ...
We report a male patient with the clinical characteristics of an OFDS (oral facial digital syndrome)...
AbstractWe report a 4.5year old Egyptian male child, fourth in the order of birth of healthy remote ...
Oral-facial-digital syndromes (OFDS) represent a heterogeneous group of rare developmental disorders...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...
We report a 2 months old boy, the first in order of birth of non-consanguineous parents, with sever...
AbstractWe report a 2months old boy, the first in order of birth of non-consanguineous parents, with...
AbstractWe report a 4month old male infant, the first in order of birth of healthy first cousin cons...
Oral-facial-digital syndrome (OFDS) is a group of disorders characterized by oral cavity malformatio...
The oral-facial-digital syndromes (OFD) are part of a great number of genetic disorders. They are cl...
We report the case of a 2.5 year old female, 2nd in order of birth of 1st cousin consanguineous marr...
Oral-facial-digital syndrome as heterogeneous developmental conditions is characterized by abnormali...
This is the final version. Available on open access from Tehran University of Medical Sciences via t...
Oro-facial-digital syndrome (OFD) is a rare congenital disorder. Its incidence in the general popula...
AbstractBackgroundMiller syndrome is one of the acrofacial dysostosis syndromes, which are character...
Copyright © 2014 Meltem Ozdemir-Karatas et al. This is an open access article distributed under the ...
We report a male patient with the clinical characteristics of an OFDS (oral facial digital syndrome)...
AbstractWe report a 4.5year old Egyptian male child, fourth in the order of birth of healthy remote ...
Oral-facial-digital syndromes (OFDS) represent a heterogeneous group of rare developmental disorders...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...