Al-Raqad syndrome

Al-Raqad syndrome is a congenital autosomal recessive syndrome discovered by Jordanian physician Mohammad Al-Raqad. It is characterized by:

• Microcephaly
• Growth delay
• Psycho-motor developmental delay
• Congenital hypotonia.

Al-Raqad syndrome is caused by mutation of DCPS gene.^[1]

• NCBI
• MalaCards: The human disease database
• The Universal Protein Resource (UniProt)

This genetic disorder article is a stub. You can help Wikipedia by expanding it.

• v
• t
• e