Sotos syndrome can be diagnosed in babies and children. It’s not a typical part of the newborn screening process in hospitals, however. Instead, doctors test for it after noticing the symptoms.

Sotos syndrome is an autosomal dominant condition characterised by a distinctive facial appearance, learning disability and overgrowth resulting in tall stature and macrocephaly. In 2002, Sotos ...

TOKYO — Sotos’ syndrome, an extremely rare genetic disorder characterized by excessive growth before and after birth, may be associated with optic disc pallor and retinal atrophy. A case ...

Sotos syndrome, also known as cerebral gigantism because of the distinctive head shape and size, is a genetic condition causing physical overgrowth during the first years of life. Ironically, this ...

This time, an international research group has revealed that mutation in the APC2 gene causes symptoms of Sotos syndrome related to the nervous system, from analyses of the Apc2-knockout mouse.

A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. Eur J Hum Genet 18 , 258–261 (2010). https://doi.org ...

This time, an international research group has revealed that mutation in the APC2 gene causes symptoms of Sotos syndrome related to the nervous system, from analyses of the Apc2-knockout mouse.

This time, an international research group has revealed that mutation in the APC2 gene causes symptoms of Sotos syndrome related to the nervous system, from analyses of the Apc2-knockout mouse.