Weaver syndrome: postnatal overgrowth with increased bone maturation
DOI:
https://doi.org/10.61651/rped.2009v62n1p34-37Keywords:
Weaver syndrome, Accelerated Bone Maturation, Craniofacial AbnormalitiesAbstract
Weaver syndrome is an extremely rare disease with unknown etiology, characterized by an accelerated postnatal growth, and special face. A case of male infant with overgrowth, increased bone maturation, moderate psychomotor retardation, hypertonic with limited movements of the limbs, and craniofacial anomalies. This is a patient with sporadic transmission, without genetic inheritance. First case reported in Latin America and number 28th world-wide.
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