Seckel Syndrome

Seckel Syndrome, also known as microcephalic primordial dwarfism, is related to microcephaly 10, primary, autosomal recessive and seckel syndrome 2, and has symptoms including seizures An important gene associated with Seckel Syndrome is ATRIP (ATR Interacting Protein), and among its related pathways/superpathways are EML4 and NUDC in mitotic spindle formation and Regulation of TP53 Activity. Affiliated tissues include bone and bone marrow, and related phenotypes are intellectual disability and delayed skeletal maturation