Seckel syndrome(English)

• a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with mental retardation, and a characteristic 'bird-headed' facial appearance. Caused by homozygous or compound heterozygous mutation in the ATR gene (601215) on chromosome 3q23
• Genetics, Pregnancy
• https://www.omi…,et al., 1997).
• https://doi.org…101.2014.956475