Novel variant related to SATB2-associated syndrome.

Background: SATB2-associated syndrome (SAS) also known as Glass syndrome is characterized by/intellectual disability and/or developmental delay coupled with absent or limited speech development. Other abnormalities can be noticed including craniofacial anomalies such as palatal and dental anomalies, behavioural problems and dysmorphic features. It is associated with pathogenic monoallelic variants of the SATB2 gene known to play a key role in brain, dental and jaw development.

[An enormous gastro-intestinal hairball (author's transl)].

A case of a gastro-duodenal hairball is reported in a neurotic 19 year old woman. The case is remarkable because of the unusual length of the foreign body and the coexistence of two gastric ulcers which led to partial gastrectomy.