We report the case of a 2.5 year old female, 2nd in order of birth of 1st cousin consanguineous marriage, with the typical features of Oral–Facial–Digital Syndrome type VI (OFDS VI) including midline pseudo cleft upper lip, sublingual nodule, molar tooth sign by MRI brain, bilateral mesoaxial polydactyly (hexadactyly), and developmental delay. The patient had self mutilations which was not reported before in OFDS VI except once.Keywords: Oral–Facial–Digital Syndrome type VI; Varadi–Papp syndrome; Self mutilation; Polydactyly; Molar tooth sign; Peudocleft li
AbstractPapillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by ...
The oral-facial-digital syndromes (OFD) are part of a great number of genetic disorders. They are cl...
The Zimmermann-Laband syndrome (ZLS) is a rare genetic disorder inherited as an autosomal dominant f...
AbstractWe report the case of a 2.5year old female, 2nd in order of birth of 1st cousin consanguineo...
We report the case of a 2.5 year old female, 2nd in order of birth of 1st cousin consanguineous marr...
AbstractWe report a 4month old male infant, the first in order of birth of healthy first cousin cons...
AbstractWe report a 2months old boy, the first in order of birth of non-consanguineous parents, with...
We report a 2 months old boy, the first in order of birth of non-consanguineous parents, with sever...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...
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...
Copyright © 2014 Meltem Ozdemir-Karatas et al. This is an open access article distributed under the ...
Oral-facial-digital syndrome (OFDS) is a group of disorders characterized by oral cavity malformatio...
We report a family having two male sibs with Simpson–Golabi–Behmel syndrome (SGBS). Both have many t...
AbstractPapillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by ...
The oral-facial-digital syndromes (OFD) are part of a great number of genetic disorders. They are cl...
The Zimmermann-Laband syndrome (ZLS) is a rare genetic disorder inherited as an autosomal dominant f...
AbstractWe report the case of a 2.5year old female, 2nd in order of birth of 1st cousin consanguineo...
We report the case of a 2.5 year old female, 2nd in order of birth of 1st cousin consanguineous marr...
AbstractWe report a 4month old male infant, the first in order of birth of healthy first cousin cons...
AbstractWe report a 2months old boy, the first in order of birth of non-consanguineous parents, with...
We report a 2 months old boy, the first in order of birth of non-consanguineous parents, with sever...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...
Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndro...
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...
Copyright © 2014 Meltem Ozdemir-Karatas et al. This is an open access article distributed under the ...
Oral-facial-digital syndrome (OFDS) is a group of disorders characterized by oral cavity malformatio...
We report a family having two male sibs with Simpson–Golabi–Behmel syndrome (SGBS). Both have many t...
AbstractPapillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by ...
The oral-facial-digital syndromes (OFD) are part of a great number of genetic disorders. They are cl...
The Zimmermann-Laband syndrome (ZLS) is a rare genetic disorder inherited as an autosomal dominant f...