Pfeiffer Syndrome type 2; A case report of cranio‐orbitofaciostenosis with bilateral choanal atresia at Muhimbili National Hospital, Tanzania

Pfeiffer Syndrome type 2; A case report of cranio‐orbitofaciostenosis with bilateral choanal atresia at Muhimbili National Hospital, Tanzania

Abstract Pfeiffer syndrome is a rare genetic disorder with heterogenous phenotype and prognosis. Due to its diverse clinical presentation, it can easily be misdiagnosed. Where genetic testing still remains a challenge, antenatal sonogram can aid in early diagnosis. The cranioorbito‐faciostenosis dem...

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Bibliographic Details
Main Authors: Insiyah Amiji, Zawadi E. Kalezi, Ashfaq Abdulshakoor, Janet F. Tarimo, Raymond Leiya, Antke Zuechner, Helga E. Naburi, Augustine Massawe, Karim P. Manji
Format: Article
Language:English
Published: Wiley 2020-09-01
Series:Clinical Case Reports
Subjects:
choanal atresia
cloverleaf shaped skull
Pfeiffer syndrome
proptosis
Online Access:https://doi.org/10.1002/ccr3.2959

Internet

https://doi.org/10.1002/ccr3.2959

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