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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.
Microretrognathia
A form of developmental hypoplasia of the mandible in which the mandible is mislocalised posteriorly.
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