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Publikováno v:
Journal of Cleft Lip Palate and Craniofacial Anomalies, Vol 5, Iss 1, Pp 56-57 (2018)
De Barsy syndrome, a rare genetic disorder, is characterized by progeroid features, cutis laxa, ocular abnormalities, growth retardation, and intellectual disability. We present a case of 1½- year-old male child with De Barsy syndrome associated wit
Publikováno v:
Journal of Cleft Lip Palate and Craniofacial Anomalies, Vol 5, Iss 1, Pp 56-57 (2018)
De Barsy syndrome, a rare genetic disorder, is characterized by progeroid features, cutis laxa, ocular abnormalities, growth retardation, and intellectual disability. We present a case of 1½- year-old male child with De Barsy syndrome associated wit
Externí odkaz:
https://doaj.org/article/c8fe2ba90a2b44cc8276e1adaa0805f9