z-logo
open-access-imgOpen Access
Rare case of “diprosopus bicephalous triophthalmus” and review of literature
Author(s) -
Panduranga Chikkannaiah,
Nishaa Prathap,
Srinivasamurthy Venkataramanappa
Publication year - 2018
Publication title -
journal of pediatric neurosciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.247
H-Index - 18
eISSN - 1998-3948
pISSN - 1817-1745
DOI - 10.4103/jpn.jpn_31_18
Subject(s) - medicine , anencephaly , craniofacial , gene duplication , anomaly (physics) , fetus , anatomy , pregnancy , genetics , psychiatry , biology , physics , gene , condensed matter physics
Diprosopus is a rare congenital anomaly, characterized by partial or complete duplication of the craniofacial structure. It constitutes 0.4% of all congenital anomalies. Complete duplications are invariably associated with systemic anomalies. Here, we present such a case of diprosopus with complete duplication of face in a 24-week-old male fetus, associated with anencephaly and spinal rachischisis. Proposed theory of embryogenesis and associated anomalies are also discussed.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here