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Ophthalmic Genet ; 34(1-2): 65-8, 2013.
Article in English | MEDLINE | ID: mdl-22697357

ABSTRACT

We describe two siblings with epiphora, telecanthus, expressionless face, thick facial skin, bulky nose and profound sensorineural hearing loss. Constellation of these features presented a phenotypic overlap with Blepharo-naso-facial syndrome (BNFS) and Nablus mask-like syndrome (NMLS). They in addition had posterior helical pits. The molecular basis of NMLS is known, while BNFS remains an elusive disorder. We report the first Indian family with features having significant overlap between the two but we attempt to summarize the frequency of reported features and bring out the most consistent features for these two syndromes for the treating clinician.


Subject(s)
Abnormalities, Multiple/diagnosis , Blepharophimosis/diagnosis , Craniofacial Abnormalities/diagnosis , Eyelids/abnormalities , Face/abnormalities , Nose/abnormalities , Abnormalities, Multiple/genetics , Blepharophimosis/genetics , Child , Child, Preschool , Comparative Genomic Hybridization , Craniofacial Abnormalities/genetics , Humans , Male , Phenotype , Siblings , Syndrome
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