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Article

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.

Journal of medical genetics - 1 Jan 2009

Lyons M J, Graham J M, Neri G, Hunter A G W, Clark R D, Rogers R C, Moscarda M, Boccuto L, Simensen R, Dodd J, Robertson S, DuPont B R, Friez M J, Schwartz C E, Stevenson R E

Abstract excerpt

BACKGROUND: FG syndrome (FGS) is an X-linked disorder characterised by mental retardation, hypotonia, particular dysmorphic facial features, broad thumbs and halluces, anal anomalies, constipation, and abnormalities of the corpus callosum. A behavioural phenotype of hyperactivity, affability, and excessive talkativeness is very frequent. The spectrum of clinical findings attributed to FGS has widened considerably...

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Source

Identifiers

PMID: 18805826
DOI: 10.1136/jmg.2008.060509

Genes

MED12

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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