Cayler syndrome is a rare pediatric condition characterized by asymmetric crying
faces and various associated anomalies. This case series study presented five
cases of Cayler syndrome, with the aim of contributing to the growing body of
knowledge about this condition. The study observed that Cayler syndrome has a
wide range of clinical presentations and associated anomalies, highlighting the
complexity of the condition. Recognizing the various phenotypic expressions of
the syndrome is crucial to ensure timely and appropriate care. The study also
observed familial cases of Cayler syndrome. Further research is needed to
explore the genetic basis of Cayler syndrome, as identifying potential causative
genetic mutations could improve the accuracy of diagnosis and provide
information for genetic counseling. Furthermore, the study found a strong
association between Cayler syndrome and congenital heart defects, emphasizing
the need for a rigorous cardiac evaluation in infants with suspected or confirmed
cases.
Keywords: Asymmetric crying faces, clinical presentations, congenital heart
defects, genetic basis, pediatric condition
