What is wolf-hirschhorn syndrome and how is it treated?

See below: Wolf–hirschhorn syndrome (whs), also known as chromosome deletion dillan 4p syndrome, pitt-rogers-danks syndrome (prds) or pitt syndrome. The most common characteristics include a distinct craniofacial phenotype (microcephaly, micrognathia, short philtrum, prominent glabella, ocular hypertelorism, dysplastic ears and periauricular tags), growth and mental retardation, muscle hypotonia, & seizures.