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Pediatric-Neurodevelopmental Disabilities Activities (210)
21-hydroxylase deficiency is an autosomal recessive disorder caused by a deficiency in one of the enzymes required for t ...
Pediatric abusive head trauma (AHT), or shaken baby syndrome, most often involves shaking, blunt impact, or a combinatio ...
Acrodermatitis enteropathica is a rare skin disorder associated with zinc deficiency that is most often seen in infants. ...
Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features (elfin-like face ...
Werdnig-Hoffmann disease is a type of spinal muscular atrophy (SMA). It is the most common type of SMA and accounts for ...