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Monosomy 5p
Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism.
Prominent forehead
Forward prominence of the entire forehead, due to protrusion of the frontal bone.
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PMID (PMCID)