FG syndrome

FG syndrome (FGS; also known as Opitz–Kaveggia syndrome) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. FG syndrome was named after the first letters of the surnames of the first patients noted with the disease.^[1] First reported by Opitz and Kaveggia in 1974,^[2] its major clinical features include intellectual disability, hyperactivity, hypotonia (low muscle tone), and a characteristic facial appearance including macrocephaly (an abnormally large head).^[3]

Characteristics

FG syndrome's major clinical features include intellectual disability, usually severe; hyperactive behavior, often with an outgoing personality; severe constipation, with or without structural anomalies in the anus such as imperforate anus; macrocephaly; severe hypotonia; a characteristic facial appearance due to hypotonia, giving a droopy, "open-mouthed" expression, a thin upper lip, a full or pouting lower lip, and partial or complete loss of the corpus callosum. About a third of reported cases of individuals with FG syndrome die in infancy, usually due to respiratory infection; premature death is rare after infancy.^[3]

Developmental Effects

Due to the agenesis (loss) of the corpus callosum, intellectual disabilities are common among individuals with FG syndrome.^[4] Motor ability is also impaired as a result of having FG syndrome and its effects on the development of neurons.^[4] During infancy, problems arise in the gastrointestinal and gastroesophageal systems of the body.^[4] The most common gastrointestinal problems include constipation from imperforated anuses and gastroesophageal reflux.^[4] Cardiopulmonary defects also contribute to roughly 60% of premature deaths in infants with FG syndrome.^[4] Of all of the congenital heart defects septal defects are the most common.^[4] After infancy, long term survival has been recorded to individuals surviving beyond the age of 50.^[4]

Genetics

Most mutations that cause FG syndrome can be found in the MED12 gene. However, mutations have also been found in FMR1, FLNA, UPF3B, CASK, MECP2, and ATRX genes.^[4] Mutations on these different genes lead to the different types of FG syndrome, all with similar characteristics.^[4] The FGS1 type mutation is the most common of the types, and is found in the MED12 gene.^[4]

Known types and affected genes include:

MED12 Gene

The MED12 gene codes for the Mediator Complex Subunit 12 protein.^[5] The mediator complex is composed of around 25 different proteins that all help with the regulation of gene activity.^[5] This mediator complex regulated gene expression by bridging interaction between RNA polymerase II and gene-specific regulating proteins such as transcription factors, repressor proteins, activator proteins, etc.^[5] Changes to this complex and the proteins associated can have a severe impact on the production of new proteins.^[5] The MED12 gene is also thought to be highly linked to neuron development as well as high usage in the cells signal transduction pathway.^[5] This explains the slowed intellectual development individuals with FG syndrome have.^[5]

History

Kim Peek (1951–2009) probably had FG syndrome.

The name of the syndrome comes from the initials of the surnames of two sisters, who had five sons with the syndrome. The first study of the syndrome, published in 1974,^[2] established that it was linked to inheritance of the X chromosome.^[6]

A 2008 study concluded that Kim Peek, who was the basis for Dustin Hoffman's character Raymond Babbitt in the movie Rain Man, probably had FG syndrome^[6] rather than autism.

See also

• Lujan–Fryns syndrome

References