MISDIAGNOSIS OF TRACHER-COLLINS SYNDROME INITIALLY ATTRIBUTED TO DRUG TERATOGENICITY: A MOROCCAN CASE REPORT
Lamzouri A, EL Rherbi A, Ratbi I, Laarabi FZ, Chahboune R, Elalaoui SC, Hamdaoui H, Bencheikh RS, Sefiani
*Corresponding Author: Afaf Lamzouri (MD, Ass. Prof.): Department of Medical Genetics and Oncogenetics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy of Tangier, BP 365 km 15 Gzenaya Tangier, Morocco. Fax: 05.39.39.21.46. Phone number: 00 212 6 10 77 79 59. Email: lamzouriafaf@hotmail.com / lamzouriafaf82@gmail.com / a.lamzouri@uae.ac.ma
page: 69
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CONCLUSION
In conclusion, it is crucial to emphasize two key
points that hold immense significance for healthcare
professionals in general, and pediatricians, in particular.
Firstly, a profound awareness of the social and psychological implications of any malformation syndrome in children
is paramount. It is essential to recognize that seeking a
genetic consultation to establish a confirmed etiological
diagnosis can significantly alleviate the prolonged social
and psychological distress that patients and their families
may endure. This step can lead to more targeted and effective interventions, ultimately improving the quality of
life for affected individuals. Secondly, healthcare practitioners must act swiftly in seeking pharmacovigilance
guidance whenever adverse events emerge after medication administration. This proactive approach is essential to
ensure a precise assessment of causality. It also safeguards
against prematurely attributing blame to the medication,
as establishing drug causation should be a diagnosis of
exclusion, requiring a thorough and meticulous process
of elimination.
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